Functionalized cyanosilane and synthesis method and use thereof

ABSTRACT

The present teachings relate to a functionalized silyl cyanide and synthetic methods thereof. As an example, the method may include adding a raw material silane and a cyanide source MCN in an organic solvent to produce the functionalized silyl cyanide in the absence of catalyst or in the presence of a metal salt catalyst. The functionalized silyl cyanide may be used in the reactions that classic TMSCN participates in, to synthesize important intermediates (e.g., cyanohydrin, amino alcohols and α-amino nitrile compounds), with improved reactivity and selectivity. The cyanosilyl ether resulted from the nucleophilic addition of functionalized silyl cyanide to aldehyde or ketone may undergo intramolecular reaction under appropriate conditions to transfer the functional groups on silicon onto the other parts of the product linked to silicon. Such a functional group transfer process may increase the synthesis efficiency and atom economy, as well as afford products unobtainable using traditional TMSCN.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a Continuation-In-Part application based on PCT/CN2016/089343, filed on Jan. 26, 2017, which claims the benefit of CN 2015104375294 and CN 2015104372756, both of which were filed on Jul. 23, 2015, the disclosures of which are fully incorporated herein by reference in their entireties.

BACKGROUND 1. Technical Field

The invention relates to technical field of organic compound processing application, specifically, to a functionalized silyl cyanide, a synthesis method and use thereof.

2. Technical Background

Nucleophilic addition reaction of cyanide to carbonyl compounds, imine and electron-deficient olefin etc. could be used for the synthesis of cyanohydrin, aminonitrile and nitrile compounds, and in particularly, the corresponding chiral products are very important chiral building block, which can be widely used in the synthesis of value-added fine chemicals, such as natural products, drug molecules, bioactive molecules and chiral ligands, etc. In addition, cyanide could undergo ring-opening reaction with epoxy, and aziridine, or participate in substitution and coupling reaction to selectively introduce cyano group. Therefore, developing new cyanating reagents has been of great interest to the chemical synthesis. Trimethylsilyl cyanide (TMSCN) is one of the most commonly used cyanating reagent, for the following advantages:1) it is more convenient and secure to use than HCN, and 2) the trimethylsilyl group can be used as a protecting group for cyanohydrin. Therefore, it is widely used in cyanation reactions, especially in catalytic enantioselective cyanation reactions. However, the use of TMSCN as the cyanating reagent has some deficiencies:

In most of TMSCN participated reactions, the trimethylsilyl is not part of the target products, which can only be discharged in the form of by-products, thus compromised the overall atomic utilization of the reactions. As shown in Scheme (1), whether in the addition reaction, ring-opening reaction or coupling reaction, the trimethylsilyl in TMSCN is eventually discharged in the form of by-products (TMSX or TMSOH).

In some reactions, the reactivity of TMSCN is low. For example, in the ring-opening reaction of TMSCN to epoxide, Jacobsen et al found that, even using 10 mol % of chiral ytterbium catalyst, the reaction still took 7 days to achieve 83% yield (Org. Lett.2000, 2, 1001).

For some substrates, a high selectivity is difficult to achieve using TMSCN. For example, we found that in the nucleophilic addition reaction of TMSCN to alkenyl ketone, the target product could only be obtained with 80% ee, even at −30° C. (J. Am. Chem. Soc. 2016, 138, 416); as shown in Scheme (3).

Therefore, there is a need to overcome the deficiencies of using TMSCN as a cyanating reagent. The present teaching aims to address those issues.

SUMMARY

The teachings disclosed herein relate provides a synthetic method for a series of novel functionalized silyl cyanide 1 with high yield by using commercially available silane compound 2 as the raw material, and commercially available MCN (including HCN or inorganic cyanides) as the cyanide source, cheap and readily available inorganic metal salt NX¹a as Lewis acid catalyst in common organic solvents. The novel functionalized silyl cyanide 1 synthesized in the invention can not only be used as highly efficient cyanating reagent to realize the nucleophilic addition reactions, ring-opening reactions, substitution reactions or coupling reactions which TMSCN participates in, but also can transfer the functional groups on the silyl group into the final product by tandem nucleophilic addition reaction/functional group transfer reaction, thus improving the overall atom utilization of the reaction. According to the functional groups on the silyl, the functionalized silyl cyanide 1 can also be used to design a series of tandem reaction, such as tandem nucleophilic addition reaction/radical addition reaction, tandem cyanosilylation reaction/ring-closing olefin metathesis reaction etc. to construct a series of silicon-containing heterocyclic compounds with new structure. In addition, the invention also provides a use of the functionalized silyl cyanide 1 in the total synthesis of the Colorado potato beetle aggregation pheromone (S)-1,3-dihydroxy-3,7-dimethyloct-6-en-2-one[(S)—CPB], as well as an intermediate compound in the synthesis.

The synthetic method for preparing the functionalized silyl cyanide 1 in the invention is as shown in Scheme (I), comprising the steps of: reacting a raw material silane compound 2 and HCN or inorganic cyanide via substitution reaction in the presence of a metal salt NX¹ _(a) (also known as Lewis acid catalyst NX¹ _(a)) as the catalyst, in an organic solvent, thereby producing the novel functionalized silyl cyanide 1;

Wherein,

FG is selected from F, Cl, Br, I, CHF₂, CHCl₂, —CH₂CH═CR₂, —CH═CR₂, and —C≡CR; wherein, —CH₂CH═CR₂, —CH═CR₂ and —C═CR are functional groups having unsaturated carbon-carbon bond; wherein, R is H, Me;

R¹ is Me, Et;

X is selected from Cl, Br, I and OTf;

n=1-5.

Preferably, FG is selected from Cl, Br, —CH₂CH═CH₂, —CH═CH₂, and —C CR; wherein R is H, Me;

R¹ is Me;

X is Cl, Br;

n=1-3.

MCN is HCN or inorganic cyanides, wherein, M=H, Li, Na, K;

preferably, MCN is selected from HCN, NaCN and KCN.

The Lewis acid NX¹ _(a) represents inorganic salt, wherein, N═Li, Na, K, Mg, Zn, X¹═Br, I, OTf, a=1-3. Preferably, NX¹ _(a) is KI, ZnI₂.

Wherein, the reaction is conducted at a temperature of −20-200° C. under a nitrogen atmosphere; preferably, the reaction is conducted at a temperature of −20-120° C. under a nitrogen atmosphere.

Wherein, the silane compound 2 is commercially available raw material; MCN is a reagent used as the cyanide source.

The metal salt catalyst NX¹ _(a) is used for catalyzing the substitution reaction between the raw material 2 and MCN.

The product 1 is the corresponding novel cyanosilylation reagent, i.e. the functionalized silyl cyanidel.

Wherein, the molar ratio of silane compound 2, MCN and catalyst NX¹ _(a) is 100-300: 150-300: 3-9; preferably, is 100-200: 150-200: 3-9; more preferably, is 150: 200: 6.

The organic solvent is one or more of N,N-dimethylformamide (DMF), N,N-dimethylacetamide, dimethyl sulfoxide (DMA), tetrahydrofuran (THF), acetonitrile (CH₃CN), dichloromethane and toluene; preferably, is DMF, CH₃CN.

The novel cyanosilylation reagent 1 is the target product, and the silane compound 2 is commercially available raw material. Wherein, FG may be halogen atom such as F, Cl, Br, I; halogenated alkyl such as CHF₂, CHCl₂, etc.; functional groups having unsaturated carbon-carbon bonds such as —CH₂CH═CR₂, —CH═CR₂, —CCR (R═H or Me) et al.; R¹ is Me, Et.

The invention also provides a functionalized silyl cyanide represented by the following Formula (1), synthesized by the aforementioned synthesis method.

Wherein,

FG is selected from F, Cl, Br, I, CHF₂, CHCl₂, —CH₂CH═CR₂, —CH═CR₂, and —CCR; wherein, —CH₂CH═CR₂, —CH═CR₂ and —C═CR are functional groups having unsaturated carbon-carbon bond; wherein, R is H, Me;

R¹ is Me, Et;

n=1-5.

Preferably, FG is selected from Cl, Br, —CH₂CH═CH₂, —CH═CH₂, —CCR; Wherein, R is H, Me;

n=1-3.

The invention also provides a use of the functionalized silyl cyanide as shown in Formula (1) for nucleophilic addition reaction, comprising racemic nucleophilic addition reaction and asymmetric nucleophilic addition reaction; comprising the step of: reacting the functionalized silyl cyanide 1a and electrophilic reagent 3 under the catalysis of a catalyst I, to synthesize compound 4 by nucleophilic addition reaction; wherein, the compound 4 is in R and/or S configuration. The process of the reaction is as shown in Scheme (II):

Wherein, the definitions of FG and n are the same as that in Scheme (I); CN is cyano group;

Y is selected from O, NBn, NCbz, NTs, NBoc, NPMP, NP(O)Ph₂, CHEWG (EWG=CN, NO₂, CO₂R, CONR₂, wherein, R=Me, Et, Ph, Bn);

R² is selected from C1-C20 alkyl, phenyl, C6-C20 substituted phenyl, naphthyl, C10-C20 substituted naphthyl, furanyl, C4-C10 substituted furanyl, thienyl, C4-C10 substituted thienyl, pyrryl, C4-C10 substituted pyrryl, pyridyl, and C5-C10 substituted pyridyl, et al.

Preferably, R² is selected from the groups consisting of the following Formula (a)˜(l): wherein, the C6-C20 substituted phenyl is as shown in Formula (a), the C10—C20 substituted naphthyl is as shown in Formula (b) and (c), the C4-C10 substituted furanyl is as shown in Formula (d) and (e), the C4-C10 substituted thienyl is as shown in Formula (f) and (g), the C4-C10 substituted pyrryl is as shown in Formula (h) and (i), the C5-C10 substituted pyridyl is as shown in Formula (j) to (l);

Wherein, for S_((b)) and S_((c)) of Formula (a) to (l), S is a substituent, and the substituent is selected from the group consisting of: same or different halogen; C1-C4 alkyl; C1-C4 alkoxyl; ester group (CO₂R, wherein, R=Me, Et, i-Pr, t-Bu, Ph, Bn); cyano group; nitro; acetal group and ketal group; b, c are the amount of the substituents, and b is an integer from 1 to 5 inclusive; c is an integer from 1 to 3 inclusive.

More preferably, R² is selected from C1-C20 alkyl, phenyl, C6-C20 substituted phenyl, naphthyl, C10-C20 substituted naphthyl, furanyl, C4-C10 substituted furanyl, thienyl, C4-C10 substituted thienyl, pyrryl, C4-C10 substituted pyrryl, pyridyl, C5-C10 substituted pyridyl, ester group (CO₂R, R=Me, Et), amide (CONR₂, R=Me, Et), et al.

Still more preferably, R² is selected from C1-C10 alkyl, phenyl, C6-C14 substituted phenyl, naphthyl, C10-C14 substituted naphthyl, furanyl, C4-C10 substituted furanyl, thienyl, C4-C10 substituted thienyl, pyrryl, C4-C10 substituted pyrryl, pyridyl, C5-C10 substituted pyridyl.

R³ is selected from H; C1-C20 alkyl; ester group (CO₂R, wherein, R=Me, Et, i-Pr, t-Bu, Ph, Bn), amide (CONR₂, R=Me, Et, CF₃), et al.

Preferably, R³ is selected from H; C1-C10 alkyl; ester group (CO₂R, wherein, R=Me, Et, t-Bu), amide (CONR₂, R=Me, Et), et al.

R⁵ is H, or silyl on the functionalized silyl cyanide. When the substrates are not the same, the corresponding products are different.

The catalyst I is a nucleophilic addition reaction catalyst, used for catalyzing the nucleophilic addition reaction of the functionalized silyl cyanide 1a to the electrophilic reagent 3.

The nucleophilic addition reaction catalyzed by the catalyst I is conducted under a nitrogen atmosphere at a temperature of −50˜150° C. while stirring until completion; preferably, the reaction temperature is −50˜50° C.

The dosage of the catalyst I is 0.001-0.5 equivalent relative to the electrophilic reagent 3; preferably, is 0.001-0.1 equivalent.

The dosage of the functionalized silyl cyanide 1a is 1.0-5.0 equivalent relative to the electrophilic reagent 3; preferably, is 1.0-2.0 equivalent.

The racemic nucleophilic addition reaction and asymmetric nucleophilic addition reaction differ in that, the catalysts are not the same, with the other reaction conditions the same:

For the racemic nucleophilic addition reaction, the catalyst I′ comprises:

1) achiral inorganic Lewis base catalyst, comprising: inorganic metal carbonate comprising K₂CO₃, Li₂CO₃, Na₂CO₃, Cs₂CO₃; carboxylate comprising KOAc, LiOAc, NaOAc, CsOAc; and phosphate comprising K₃PO₄, Li₃PO₄, Na₃PO₄, et al.;

2) achiral organic Lewis base catalyst, such as: tertiary amine compounds comprising Et₃N, DABCO, i-Pr₂NEt; piperidine, pyridine derivatives comprising DMAP, N-methyl piperidine, oxynitride such as

et al.;

3) achiral Lewis acid catalyst, comprising: metal salt comprising ZnI₂, KI, Zn(OTf)₂, TiCl₄.

For the asymmetric nucleophilic addition reaction, the catalyst I″ are common chiral catalysts suitable for silylcyanation reaction, comprising:

Chiral Lewis acid catalyst, chiral Lewis base catalyst, and chiral bifunctional catalyst having both Lewis acid functional group and Lewis base functional group co-existing in one molecule, and a variety of catalyst systems formed by chiral catalysts and achiral catalysts. Specifically, the catalyst I″ contains the catalysts as shown in the following Formula (IC1)˜Formula (IC6):

Wherein, in Formula (IC1), R⁴ is H, CH₃, OEt, Ot-Bu;

In Formula (IC2), X¹ is OTf, NTf₂;

In Formula (IC5), n is 1-5.

For the nucleophilic addition reaction, the general procedure comprises the following steps: the catalyst I, the raw material, an anhydrous solvent and the electrophilic reagent 3 are added into a dry Schlenk tube. The mixture is stirred and then added the functionalized silyl cyanide 1a. The progress of the reaction is monitored by TLC (thin-layer chromatography). After full consumption of the raw material, the reaction mixture is subject to column chromatography directly, and the yield could be determined.

The invention also provides the use of the functionalized silyl cyanide for synthesizing alcohols compounds bearing substituted ketone moiety, comprising racemic alcohols compounds and chiral alcohols compounds, via tandem nucleophilic addition reaction/functional group transfer reaction; comprising the step of: contacting functionalized silyl cyanide 1aa with a carbonyl compound 3a via nucleophilic addition reaction to provide an intermediate 4a which undergoes an intramolecular nucleophilic addition reaction promoted by base I and a hydrolysis reaction promoted by acid I; thereby producing an alcohols compounds 5 bearing substituted ketone moiety; the alcohols compounds 5 is in R and/or S configuration; the reaction process is as shown in Scheme (III):

Wherein, the definition of R² and R³ are the same as that in Scheme (II); CN is cyano group.

The catalyst I is used for catalyzing the nucleophilic addition reaction between the compound of Formula (1aa) and the compound of Formula (3a).

For the synthesis of racemic alcohols compounds, the catalyst I′ used in the nucleophilic addition reaction is the same as the catalyst I′ used in the racemic nucleophilic addition reaction as shown in Scheme (II); and the dosage of the catalyst I′ can refer to that for Scheme (II).

For the synthesis of chiral alcohols compounds, the catalyst I″ used in the nucleophilic addition reaction is the same as the catalyst I″ used in the asymmetrical nucleophilic addition reaction as shown in Scheme (II); the dosage of the catalyst I″ can refer to that for Scheme (II).

The reaction conditions of the nucleophilic addition reaction in the tandem nucleophilic addition reaction/functional group transfer reaction is the same as that for Scheme (II). The dosage of the corresponding compounds can refer to that for Scheme (II).

Z is Cl, Br. The base I is a strong base for removing hydrogen adjacent to FG, which is selected from LDA, NaHMDS, KHMDS; preferably, is LDA. The dosage of the base I is 1.0-3.0 equivalent relative to the intermediate compound 4a; preferably, is 1.0-2.0 equivalent.

The intramolecular nucleophilic attack reaction promoted by the base I is conducted under a temperature of −80-50° C., while stirring for completion.

The acid I is an acidic catalyst used for hydrolyzing C—Si and C═N bond, which is selected from hydrochloric acid, sulfuric acid, acetic acid; preferably, is hydrochloric acid. The dosage of the acid I is 10-50 equivalent relative to the intermediate compounds 4a; preferably, is 10-20 equivalent.

For tandem nucleophilic addition reaction/functional group transfer reaction, the general procedure is: the catalyst I, the raw material of 3a and a corresponding solvent were added into a dry Schlenk tube (25 mL). The mixture was added with 1aa after being stirred for 0.5 h. The progress of the reaction was monitored by TLC analysis. After the consumption of the raw material 3a is complete, the crude product 4a was obtained by filtering the reaction mixture through a5 cm silica gel column, eluting with Et₂O, and removing solvent under reduced pressure. The crude product 4a was transferred to a dry Schlenk tube (25 mL) and dissolved with anhydrous THF. The resulting solution was added with a base I dropwise slowly. The progress of the reaction was monitored by TLC analysis. After the consumption of 4a was complete, the reaction was quenched by acid I. The resulting mixture was extracted three times by EtOAc. Product 5 as shown in Scheme (III) was obtained by combing the organic phase, and rotary evaporating to remove the solvent followed by column chromatography directly.

In one exemplary example, the invention also provides a use of the functionalized silyl cyanide for total synthesis of Colorado potato beetle aggregation pheromone (S)-1,3-dihydroxy-3,7-dimethyloct-6-en-2-one[(S)—CPB], comprising the following steps: contacting the functionalized silyl cyanide 1aa and carbonyl compound 6 in the presence of the catalyst I via nucleophilic addition reaction, thereby producing an intermediate 7;

Performing an intramolecular nucleophilic attack of the intermediate 7 under the action of LDA followed by a hydrolyzation in the presence of hydrochloric acid to afford a compound 8;

Reacting the compound 8 and KOAc by substitution reaction followed by a hydrolyzation in the presence of K₂CO₃, thereby producing the [(S)—CPB]; the reaction process is as shown in the following Scheme (IV),

Wherein, Z is Cl, Br;

The dosage of LDA is 1.0-3.0 equivalent relative to the intermediate compounds 7.

The invention also provides a new structural compound, i.e. an intermediate compound in the synthesis of (S)—CPB, which is represented by Formula (7),

Wherein: Z is Cl, Br.

The invention also provides a use of the functionalized silyl cyanide in tandem cyanosillalation reaction/ring-closing olefin metathesis reaction comprising racemic cyanosillalation reaction/ring-closing olefin metathesis reaction and asymmetric cyanosillalation reaction/ring-closing olefin metathesis reaction; comprising the following steps:

Reacting functionalized silyl cyanide lab and an alkenyl ketone 9 by cyanosillalation reaction in the presence of the catalyst I to produce an intermediate 10;

Performing an intramolecular ring-closing olefin metathesis reaction of the intermediate compound 10 in the presence of Grubbs I, thereby producing a silicon-containing heterocyclic compound 11;

Wherein, the silicon-containing heterocyclic compound 11 is in R and/or S configuration; and the process of the reaction is shown as in the following Scheme (V):

Wherein, n is 0, 1, or 2;

For racemic cyanosillalation reaction/ring-closing olefin metathesis reaction, the catalyst I used for the cyanosillalation reaction is K₂CO₃;

For asymmetric cyanosillalation reaction/ring-closing olefin metathesis reaction, the catalyst I used for the cyanosillalation reaction is IC1; and

R⁶ is H, Me, Et, Ph.

The invention also provides a use of the functionalized silyl cyanide for epoxy ring-opening reaction/functional group transfer reaction, comprising the following steps:

Reacting the functionalized silyl cyanide 1aa and an epoxy compound 12 in the presence of a catalyst I by epoxy ring-opening reaction to produce an intermediate 13;

Performing an intramolecular nucleophilic attack of the intermediates compound 13 under the promotion of LDA followed by a hydrolyzation under the hydrolysis of hydrochloric acid to afford an alcohol compound 14;

Wherein, the alcohol compound 14 is in R and/or S configuration; and the epoxy ring-opening reaction/functional group transfer reaction comprises racemic epoxy ring-opening addition reaction/functional group transfer reaction and asymmetric epoxy ring-opening reaction/functional group transfer reaction; and the process of the reaction is as shown in the following Scheme (VI):

Wherein, the definitions of Z and the catalyst I are the same as that in Scheme (III); CN is cyano group;

R⁷ is Me, Ph, Bn, BnCH₂,

R⁸ and R⁹ are H, Me, Et, Allyl; and R⁸ and R⁹ can be the same or different.

The present invention has the advantages that all the reagents used in the invention are commercially available, the source of the raw materials is wide, the raw materials are cost-effective, each reagent is stable under normal temperature and pressure, the operation are convenient, the catalyst used in the invention is relatively stable to air and moisture, the reactions are suitable for large-scale production; therefore the functionalized silyl cyanide synthesized in the invention has broad application prospect. The functionalized silyl cyanide could be used in the reactions which classic TMSCN participates in, to synthesize important intermediates such as cyanohydrin, amino alcohols and α-amino nitrile compounds, with better reactivity and selectivity, etc. Especially the products resulted from the nucleophilic addition reaction of functionalized silyl cyanide to carbonyl compounds could undergo intramolecular reaction under appropriate conditions to transfer the functional groups on silicon onto the other parts which is linked to silicon of the product. Such a functional group transfer process could not only increase the synthesis efficiency and atom economy, but also afford products which cannot be obtained by traditional TMSCN reagent. The asymmetric synthesis of (S)-1,3-dihydroxy-3,7-dimethyloct-6-en-2-one [(S)—CPB], was realized from commercially available 6-methylhept-5-en-2-one (CAS: 110-93-0), and the functionalized silyl cyanide synthesized in the invention. The compound (S)—CPB synthesized in the present invention is a kind of aggregation pheromones secreted by male Colorado potato beetle, which is a potential effective hormone-like pesticide for both sexes of Colorado potato beetle.

Additional novel features will be set forth in part in the description which follows, and in part will become apparent to those skilled in the art upon examination of the following or may be learned by production or operation of the examples. The novel features of the present teachings may be realized and attained by practice or use of various aspects of the methodologies, instrumentalities and combinations set forth in the detailed examples discussed below.

DETAILED DESCRIPTION

In the following detailed description, numerous specific details are set forth by way of examples in order to provide a thorough understanding of the relevant teachings. However, it should be apparent to those skilled in the art that the present teachings may be practiced without such details. In other instances, well known methods, procedures, components, and/or circuitry have been described at a relatively high-level, without detail, in order to avoid unnecessarily obscuring aspects of the present teachings.

The present disclosure generally relates to systems, methods, medium, and other implementations directed a series of novel functionalized silyl cyanide 1 are designed and synthesized in the present invention. In principle, the functionalized silyl cyanide 1 could participate in all reactions which could be realized by TMSCN. In principle, the functionalized silyl cyanide 1 could participate in all reactions which could be realized by TMSCN. In addition, the functionalized silyl cyanide 1 also has the following three advantages:

First, the introduction of the functional group (FG) has certain influence on the steric and electrical property of the silicon atom, and makes the functionalized silyl cyanide 1 more reactive or selective than TMSCN.

In nucleophilic addition reaction of the functionalized silyl cyanide 1 to carbonyl compounds, the adduct could occur intramolecular reaction under appropriate conditions, to transfer the functional groups on the silyl into the final product. It not only enables the utilization of the functional groups on the silyl, thus improves the overall atomic utilization of the reaction, but also realizes the conversions which are difficult to be achieved in intermolecular fashion.

The invention now being generally described, it will be more readily understood by reference to the following examples which are included merely for purpose of illustration of certain aspects and examples of the present invention, and are not intended to limit the invention.

1) Conversion from Compound 2a to Compound 1aaa (Table 1)

General procedure 1: a newly distilled 2a (100-300 mmol), MCN (150-300 mmol), a catalyst NX¹ _(a) (3-9 mmol) and an organic solvent (100 mL) were added into a dry three-necked flask (250 mL). The mixture was stirred at a temperature shown in Table 1. The progress of the reaction was monitored by GC analysis. After the consumption of the raw material 2a was complete, 1aaa as shown in Scheme (Ia) was obtained through reduced pressure distillation.

The specific experimental operations of the examples 1-17 are referred to general procedure 1. The specific reaction conditions and yield of each example are shown in Table 1. Wherein, 2a in Scheme (Ia) represents 2aa-2ad in Table 1 respectively.

TABLE 1 Specific reaction conditions and yields of the examples 1-17. 2a (X) (mmol)/MCN Temperature Time Yield Example (mmol)/NX¹ _(a) (mmol) Solvent (° C.) (h) (%) 1 2aa Cl (150)/HCN (200)/KI THF 0 48 66 (6) 2 2aa Cl (150)/LiCN (200)/KI toluene 150 36 37 (6) 3 2aa Cl (150)/NaCN (200)/KI THF 80 24 68 (6) 7 2aa Cl (150)/NaCN (200)/LiI DMA 150 36 34 (6) 8 2aa Cl (100)/NaCN (150)/NaI THF 100 36 66 (6) 9 2aa Cl (100)/NaCN THF 80 36 37 (150)/MgI₂ (6) 10 2aa Cl (100)/NaCN THF 80 36 74 (150)/ZnI₂ (6) 11 2aa Cl (300)/NaCN (300)/KI DMF 120 72 67 (6) 12 2aa Cl (200)/NaCN (250)/KI DMF 120 72 73 (3) 13 2aa Cl (200)/NaCN (150)/KI DMF −20 30 40 (9) 14 2ab Br (100)/NaCN (150)/KI THF 80 34 68 (6) 15 2ac I (100)/NaCN (150)/KI THF 80 24 66 (6) 16 2ad OTf (100)NaCN THF 80 72 35 (150)/KI (6) 17 2ad OTf (100)NaCN CH₃CN 25 48 65 (150)KI (6)

The characterization of compound 1aaa is as follows:

¹H NMR (400 MHz, CDCl₃): 2.96 (s, 2H), 0.48 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 124.63, 26.94, −4.73;

2) Conversion from Compound 2 to Compound 1 (Table 2)

General procedure 2: a newly distilled halogenated silane 2 (150 mmol), NaCN (200 mmol), catalyst ZnI₂ (6 mmol) and an organic solvent (100 mL) were added into a dry 250 mL three-necked flask. The mixture was stirred at a temperature shown in Table 2. The progress of the reaction was monitored by GC analysis. After the full consumption of the raw material halogenated silane 2, compound 1 as shown in Scheme (Ib) was obtained by reduced pressure distillation.

The specific experimental operations of the examples 18-37 are referred to general procedure 2. The specific reaction conditions and yield of each example are shown in Table 2. Wherein, 2 in Scheme (Ib) represents 2b-2m in Table 2, and 1 represents 1aab-1abd in Table 2 respectively.

TABLE 2 Specific reaction conditions and yields of the examples 18-37. Ex- Temper- Product/ am- ature Time Yield ple 2 Solvent (° C.) (h) (%) 18

THF 80 48 1aab/66 19 2b DMA 150 24 1aab/78 20 2b CH₃CN 100 24 1aab/77 21

THF 80 36 1aba/67 22 2c DMA 150 36 1aba/34 23 2c CH₃CN 100 36 1aba/37 24

THF 80 36 1abb/44 25 2d DMA 150 72 1abb/73 26 2d CH₃CN 100 72 1abb/56 27

THF 80 34 1aca/68 28 2e DMA 150 72 1aca/35 29 2e CH₃CN 100 48 1aca/77 30

CH₃CN 100 48 1bba/75 31

CH₃CN 80 48 1ada/42 32

CH₃CN 80 24 1adb/71 33

CH₃CN 80 24 1aea/74 34

CH₃CN 80 24 1aeb/49 35

CH₃CN 80 24 1abc/67 36

CH₃CN 80 24 1aec/46 37

CH₃CN 80 24 1abd/58

The characterizations of 1aab-1abd are as follows:

¹H NMR (400 MHz, CDCl₃): 3.3 (s, 2H), 0.38 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 128.23, 27.89, −4.78;

¹H NMR (400 MHz, CDCl₃): 5.42 (d, 1H), 5.36 (s, 1H), 5.16 (d, 1H), 0.40 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 138.0, 124.9, 118.9, −4.05;

¹H NMR (400 MHz, CDCl₃): 5.35 (dd, 1H), 5.24 (m, 2H), 2.08 (t, 2H), 0.43 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 135.0, 121.7, 119.8, 12.9, −4.09;

¹H NMR (400 MHz, CDCl₃): 4.96 (s, 1H), 0.58 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 128.6, 56.7, −6.73.

¹H NMR (400 MHz, CDCl₃): 5.14 (dd, 1H), 5.05 (m, 2H), 0.78 (t, 6H), 0.43 (q, 4H); ¹³C NMR (100 MHz, CDCl₃): δ 128.0, 115.7, 110.1, 12.9, −3.78;

¹H NMR (400 MHz, CDCl₃): 5.4 (t, 1H), 1.37 (m, 2H), 0.08 (d, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 117.8, 115.5, 22.1, −2.6;

¹H NMR (400 MHz, CDCl₃): 5.3 (t, 1H), 1.36 (m, 2H), 0.08 (d, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 116.8, 112.6, 25.1, −2.7;

¹H NMR (400 MHz, CDCl₃): 2.81 (s, 1H), 0.13 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 117.3, 90.5, 89.5, 0.6;

¹H NMR (400 MHz, CDCl₃): 2.83 (s, 1H), 2.31 (t, 2H), 1.18 (t, 2H), 0.10 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 117.5, 86.2, 69.7, 13.9, 13.6, −2.8;

¹H NMR (400 MHz, CDCl₃): 5.22 (dd, 1H), 2.07 (d, 2H), 1.82 (m, 3H), 1.74 (d, 3H), 0.10 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 132.5, 120.3, 118.5, 28.0, 17.9, 11.4, −2.3;

¹H NMR (400 MHz, CDCl₃): 2.22 (t, 2H), 2.03 (s, 3H), 1.22 (t, 2H), 0.11 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 122.0, 83.3, 78.5, 14.0, 11.9, 3.7, −2.9;

¹H NMR (400 MHz, CDCl₃): 5.82 (dd, 1H), 5.07 (d, 1H), 5.00 (d, 1H), 2.19 (m, 2H), 1.39 (m, 2H), 1.30 (m, 2H), 1.04 (t, 2H), 0.10 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 139.4, 119.3, 118.8, 33.8, 32.0, 23.3, 15.4, −2.3.

3) Nucleophilic Addition Reaction of Functionalized Silyl Cyanide 1aaa to Aldehydes or Ketones (Table 3).

General procedure 3: a catalyst I, aldehyde or ketone 3a (1.0 mmol) and corresponding solvent (1 mL) were added into a dry Schlenk tube (25 mL). After being stirred at a corresponding temperature for 0.5 h, 1aaa (2.0 mmol) was added to the mixture. The reaction process was monitored by TLC analysis. After full consumption of raw material 3a, 4a as shown in Scheme (IIa) was obtained by conventional post-treatment followed by column chromatography, or by column chromatography directly.

The specific experimental operations of the examples 38-115 are referred to general procedure 3. The specific reaction conditions and yield of each example are shown in Table 3.

TABLE 3 Specific reaction conditions and yields of the examples 38-115. Ex- Product/ am- Catalyst I Temper- Yield (%)/ ple R² R³ (mol %) Solvent ature Ee (%) 38 C₆H₅ H Li₂CO₃ (5) CH₃CN 25 4aa/76/— 39 C₆H₅ Me Na₂CO₃ (5) DMF 25 4ab/88/— 40 C₆H₅ Et K₂CO₃ (5) DMSO 25 4ac/85/— 41 C₆H₅ i-Pr K₂CO₃ (25) CH₃CN 50 4ad/90/— 42 C₆H₅

K₂CO₃ (25) CH₃CN 50 4ae/92/— 43 C₆H₅ CO₂Me KOAc (25) CH₃CN 25 4af/95/— 44 C₆H₅ CO₂Bn KOAc (25) CH₃CN 25 4ag/79/— 45 C₆H₅ CONMe₂ CsOAc (25) CH₃CN 25 4ah/83/— 46 C₆H₅ CONEt₂ LiOAc (25) THF 50 4ai/85/— 47 C₆H₅ Cy KOAc (50) CH₃CN 50 4aj/88/— 48 C₆H₅

KOAc (25) DMF 25 4ak/79/— 49 C₆H₅

K₂CO₃ (15) THF 25 4al/77/— 50 C₆H₅

K₂CO₃ (15) CH₃CN 80 4am/75/— 51 C₆H₅

K₂CO₃ (15) DMF 25 4an/69/— 52 4-Cl—C₆H₄ Me Et₃N (5) THF 40 4ao/88/— 53 3-Cl—C₆H₄ Me

toluene 50 4ap/85/— 54 4-F—C₆H₄ Me Et₃N (25) CH₂Cl₂ 25 4ar/81/— 55 4-Br—C₆H₄ Me (i-Pr)₂NEt (25) CH₃CN 25 4as/81/— 56 3,4-Cl₂—C₆H₃ Et Et₃N (25) CH₂Cl₂ 25 4at/60/— 57 2,4,6-Me₂—C₆H₂ H

  DMAP (30) CH₃CN 50 4au/90/— 58 4-NO₂—C₆H₄ Me

DMF 25 4av/85/— 59 4-Et—C₆H₄ Me K₂CO₃ (25) THF 0 4aw/85/— 60 4-Me—C₆H₄ H K₂CO₃ (15) THF 0 4ax/82/— 61 Cy H Zn(OTf)₂ (0.1) CH₃CN 25 4ay/85/— 62 Cy Me K₂CO₃ (1) DMF 50 4az/97/— 63

Me K₂CO₃ (5) THF 50 4aaa/80/— 64

H K₂CO₃ (2.5) toluene 10 4aab/92/— 65

H K₃PO₄ (2.5) CH₂Cl₂ 10 4aac/90/— 66

H Na₂PO₄ (2.5) DMF 25 4aad/75/— 67

Me K₂CO₃ (10) THF 25 4aae/95/— 68

Me K₂CO₃ (10) CH₃CN 25 4aaf/89/— 69

Me KI (10) DMF 25 4aag/91/— 70 Bn Me K₂CO₃ (5) THF 50 4aah/93/— 71

H K₂CO₃ (2.5) CH₃CN 25 4aai/88/— 72

Me TiCl₄ (0.5) toluene 0 4aaj/75/— 73

Me ZnI₂ (0.5) CH₃CN 25 4aak/84/— 74

Me TiCl₄ (0.5) toluene 0 4aal/79/— 75

Me ZnI₂ (0.5) CH₃CN 25 4aam/85/— 76

Me KI (2.5) CH₃CN 50 4aan/85/— 77 BnCH₂ Me K₂CO₃ (2) CH₃CN 50 4aao/95/— 78

Me K₂CO₃ (2.5) THF 25 4aap/85/— 79

Me K₂CO₃ (2.5) THF 25 4aaq/90/— 80 t-Bu H Zn(OTf)₂ (1) toluene 25 4aar/94/— 81 Et H Zn(OTf)₂ (1) toluene 25 4aas/80/— 82 i-Pr H Zn(OTf)₂ (1) toluene 25 4aat/87/— 83 C₆H₅ Me IC1 (10) (R⁴ = Me) CH₂Cl₂ 0 4ab/88/85 84 C₆H₅ Et IC1 (10) (R⁴ = OEt) Et₂O 0 4ac/85/83 85 C₆H₅ i-Pr IC1 (10) (R = Ot—Bu) Et₂O 0 4ad/90/75 86 C₆H₅

IC1 (20) (R = OEt) Et₂O 0 4ae/92/60 87 C₆H₅ CO₂Me IC4 (10) toluene 25 4af/95/77 88 C₆H₅ CONMe₂ IC4 (20) toluene 25 4ah/83/80 89 C₆H₅ Cy IC6 (10) CH₂Cl₂ 20 4aj/88/90 90 C₆H₅

IC1 (10) (R⁴ = OEt) CH₂Cl₂ 25 4ak/79/95 91 C₆H₅

IC1 (10) (R⁴ = OEt) CH₂Cl₂ 25 4al/77/86 92 C₆H₅

IC1 (10) (R⁴ = OEt) CH₂Cl₂ 25 4an/69/80 93 4-Cl—C₆H₄ Me IC2 (10) (X¹ = NTf₂) toluene −40   4ao/88/94 94 3-Cl—C₆H₄ Me IC2 (10) (X¹ = NTf₂) toluene −40   4ap/85/92 95 2-Cl—C₆H₄ H IC2 (10) (X¹ = OTf) THF −50   4aq/87/84 96 4-F—C6H4 Me IC2 (10) (X¹ = NTf₂) CH₂Cl₂ −40   4ar/81/90 97 4-Br—C₆H₄ Me IC2 (10) (X¹ = NTf₂) toluene −40   4as/81/89 98 3,5-Cl₂—C₆H₃ H IC2 (10) (X¹ = OTf) THF −40   4at/95/90 99 4-NO₂—C₆H₄ Me IC1 (10) (R⁴ = OEt) toluene −25   4av/85/97 100 4-Me—C₆H₄ H IC2 (10) (X¹ = OTf) CH₂Cl₂ −25   4ax/82/88 101 Cy H IC2 (0.1) (X¹ = OTf) THF 25 4ay/85/94 102 Cy Me IC1 (10) (R⁴ = OEt) Et₂O −50   4az/97/95 103

Me IC3 (10) toluene 10 4aaa/80/93 104

H IC2 (0.1) (X¹ = NTf₂) toluene −50   4aab/92/84 106

Me IC1 (10) (R⁴ = OEt) Et₂O −30   4aaf/89/94 107

Me IC1 (10) (R⁴ = OEt) Et₂O −30   4aag/91/92 108 Bn Me IC1 (10) (R⁴ = OEt) Et₂O −30   4aah/93/97 109

Me IC1 (10) (R⁴ = OEt) Et₂O −10   4aaj/75/82 110

Me IC1 (10) (R⁴ = OEt) Et₂O −30   4aak/84/84 111

Me IC1 (10) (R⁴ = Ot—Bu) toluene −50   4aal/79/85 112 BnCH₂ Me IC1 (10) (R⁴ = OEt) Et₂O −30   4aao/95/96 113 t-Bu H IC2 (0.1) (X¹ = OTf) THF 25 4aar/94/94 114 Et H IC2 (0.1) (X¹ = OTf) THF 25 4aas/80/80 115 i-Pr H IC2 (0.1) (X¹ = OTf) THF 25 4aat/87/89

The characterizations of 4aa-4aat are as follows:

¹H NMR (400 MHz, CDCl₃): δ 7.38-7.36 (m, 5H), 5.51 (s, 1H), 3.67 (dd, 2H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 133.7, 128.8, 128.0, 127.5, 118.2, 34.6, −0.4;

¹H NMR (400 MHz, CDCl₃): δ 7.04-7.35 (m, 5H), 3.47 (dd, 2H), 1.87 (s, 3H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 136.7, 128.9, 128.0, 126.5, 119.2, 35.2, 30.9, −0.3;

¹H NMR (400 MHz, CDCl₃): δ 7.40-7.36 (m, 5H), 3.46 (dd, 2H), 1.87 (q, 2H), 0.87 (t, 2H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 146.7, 128.8, 126.0, 125.5, 119.0, 35.2, 32.9, 4.2, −0.4;

¹H NMR (400 MHz, CDCl₃): δ 7.49-7.32 (m, 5H), 2.72 (s, 2H), 2.66 (s, 1H), 0.90 (s, 6H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.84, 127.94, 127.68, 127.30, 121.50, 77.78, 41.09, 21.02, 16.79, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.47-7.32 (m, 5H), 5.82 (dd, 1H), 5.07-5.02 (m, 2H), 3.47 (dd, 2H), 2.66 (dd, 2H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 137.86, 132.96, 128.69, 127.71, 127.36, 121.57, 118.52, 85.81, 44.11, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.49-7.38 (m, 10H), 5.34 (s, 2H), 2.74 (dd, 2H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 162.33, 133.85, 130.96, 128.17, 127.75, 119.13, 71.2, 62.33, 52.61, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.49-7.38 (m, 5H), 3.67 (s, 3H), 2.72 (dd, 2H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 161.67, 137.56, 133.85, 130.96, 129.01, 128.19, 128.17, 128.16, 127.75, 119.13, 71.2, 67.31, 62.61, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.42-7.34 (m, 5H), 3.44 (s, 6H), 2.59 (dd, 2H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 159.67, 131.22, 130.37, 129.41, 128.92, 111.80, 71.9, 64.00, 36.87, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.40-7.34 (m, 5H), 3.44 (s, 6H), 2.52 (dd, 2H), 1.08 (t, 6H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 163.66, 131.22, 130.37, 129.41, 128.92, 111.80, 71.9, 62.78, 43.22, 21.02, 13.15, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.40-7.36 (m, 5H), 2.52 (dd, 2H), 1.78-1.43 (m, 11H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.01, 127.85, 127.54, 127.26, 121.44, 71.96, 44.87, 71.3, 27.52, 25.89, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.38-7.30 (m, 5H), 6.20 (dd, 1H), 5.04-4.98 (m, 2H), 2.56 (dd, 2H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 137.94, 134.89, 129.12, 128.58, 127.86, 121.48, 121.27, 71.2, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.40-7.30 (m, 5H), 6.10 (dd, 1H), 5.55 (m, 1H), 2.56 (dd, 2H), 2.05 (d, 2H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 134.42, 133.10, 130.59, 129.62, 128.11, 127.75, 121.45, 71.2, 21.02, 19.10, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.43-7.35 (m, 5H), 6.10 (s, 1H), 2.56 (dd, 2H), 2.05 (s, 3H), 1.98 (s, 3H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 146.94, 134.04, 130.20, 127.69, 124.59, 121.43, 71.2, 25.84, 21.02, 19.65, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.45-7.35 (m, 5H), 2.56 (dd, 2H), 1.88 (s, 3H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 132.03, 130.95, 128.11, 126.84, 104.69, 95.94, 78.15, 71.5, 21.02, 7.30, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.50-7.38 (m, 5H), 2.83 (dd, 2H), 1.88 (s, 3H), 0.31 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.01, 135.12, 129.11, 126.12, 120.96, 71.55, 33.34, 29.57, −2.04, −2.12;

¹H NMR (400 MHz, CDCl₃): δ 7.54-7.35 (m, 5H), 2.85-2.80 (dd, 2H), 1.88 (s, 3H), 0.34 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 143.45, 135.01, 130.23, 129.31, 125.00, 122.86, 120.85, 71.48, 33.33, 29.54, −2.04, −2.12;

¹H NMR (400 MHz, CDCl₃): δ 7.58-7.36 (m, 5H), 2.87-2.79 (dd, 2H), 1.89 (s, 3H), 0.34 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 145.47, 136.01, 131.25, 129.71, 123.09, 121.86, 120.80, 71.48, 33.33, 29.54, −2.04, −2.12;

¹H NMR (400 MHz, CDCl₃): δ 7.52-7.38 (m, 5H), 2.81 (dd, 2H), 1.86 (s, 3H), 0.29 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 162.78, 136.32, 129.30, 123.36, 115.61, 72.39, 31.71, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.56-7.42 (m, 5H), 2.83 (dd, 2H), 1.86 (s, 3H), 0.32 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.54, 132.07, 126.40, 123.22, 120.89, 71.58, 33.30, 29.56, −2.04, −2.12;

¹H NMR (400 MHz, CDCl₃): δ 7.50 (s, 1H), 7.66-7.18 (m, 2H), 2.86-2.80 (dd, 2H), 1.87 (q, 2H), 0.90 (t, 3H), 0.30 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 135.27, 134.72, 131.86, 127.12 (d, J=8.0 Hz), 126.86, 121.95, 86.43, 38.52, 21.02, 7.77, −0.62.

¹H NMR (400 MHz, CDCl₃): δ 6.84 (s, 2H), 5.50 (s, 1H), 2.63 (dd, 2H), 2.38 (s, 6H), 2.30 (s, 3H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.28, 140.06, 129.81, 126.37, 118.63, 57.44, 28.43, 21.83, 20.50, −1.86.

¹H NMR (400 MHz, CDCl₃): δ 8.30-7.75 (m, 4H), 2.90 (dd, 1H), 1.92 (s, 3H), 0.38 (s, 3H), 0.36 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 148.30, 148.16, 125.78, 124.19, 120.38, 71.32, 33.32, 29.42, −1.95, −2.07;

¹H NMR (400 MHz, CDCl₃): δ 7.31-7.05 (dd, 4H), 2.90 (dd, 1H), 2.60 (q, 3H), 1.82 (s, 3H), 1.25 (t, 3H), 0.30 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 143.43, 137.34, 127.08, 123.79, 123.36, 72.39, 31.71, 27.82, 21.02, 13.19, −1.62.

¹H NMR (400 MHz, CDCl₃): δ 7.20-7.00 (dd, 4H), 2.90 (dd, 1H), 2.30 (s, 3H), 1.82 (s, 3H), 0.30 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 138.02, 137.60, 128.16, 127.40, 123.36, 72.39, 31.71, 21.09 (d, J=15.7 Hz), −1.62.

¹H NMR (400 MHz, CDCl₃): δ 4.20 (d, 1H), 2.97 (dd, 2H), 1.90 (m, 1H), 1.53-1.27 (m, 10H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 118.88, 65.71, 39.88, 28.93, 28.43, 25.92, 25.57, −1.86;

¹H NMR (400 MHz, CDCl₃): δ 2.87 (dd, 2H), 1.96 (d, 1H), 1.84-1.81 (m, 3H), 1.69 (d, J=10.8 Hz, 1H), 1.56 (s, 3H), 1.52-1.48 (m, 1H), 1.26-1.07 (m, 5H), 0.38 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 121.55, 73.61, 48.41, 29.91, 27.30, 27.06, 26.27, 26.00, 25.93, −1.78, −1.90;

¹H NMR (400 MHz, CDCl₃): δ 8.18 (s, 1H), 8.05-7.95 (m, 2H), 7.54-7.42 (m, 4H), 5.48 (s, 1H), 2.85 (dd, 1H), 0.31 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 138.44, 133.41, 132.87, 129.10, 128.49, 127.78, 127.05, 126.96, 123.90, 122.16, 121.35, 72.34, 33.28, 29.72, −2.06, −2.13;

¹H NMR (400 MHz, CDCl₃): δ 8.05 (s, 1H), 7.91-7.85 (m, 3H), 7.60 (m, 1H), 7.55-7.53 (m, 2H), 2.80 (dd, 1H), 1.97 (s, 3H), 0.31 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 136.00, 132.47, 130.51, 128.89, 128.45, 128.25, 127.61, 127.25, 127.01, 122.81, 118.37, 60.96, 28.43, −1.96;

¹H NMR (400 MHz, CDCl₃): δ 8.05-7.95 (m, 2H), 7.51-7.43 (m, 4H), 5.50 (s, 1H), 2.80 (dd, 1H), 2.45 (s, 3H), 0.31 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 136.72, 134.82, 134.15, 133.63, 129.61, 128.29, 127.93, 127.65, 121.64, 119.02, 117.08, 61.42, 28.43, 21.71, −1.86;

¹H NMR (400 MHz, CDCl₃): δ 8.08 (s, 1H), 7.99-7.93 (m, 2H), 7.38 (s, 1H), 7.05-6.99 (m, 2H), 2.83 (dd, 2H), 2.46 (s, 3H), 1.87 (s, 3H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 137.13, 134.15, 133.36, 133.04, 128.78, 128.22, 126.76, 126.20, 126.02, 122.72, 117.76, 60.00, 28.43, 20.35, −1.86;

¹H NMR (400 MHz, CDCl₃): δ 8.05 (s, 1H), 7.91-7.85 (m, 3H), 7.60 (m, 1H), 7.55-7.53 (m, 2H), 2.80 (dd, 1H), 1.97 (s, 3H), 0.31 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 135.61, 134.64, 133.51, 131.21, 130.41, 127.93, 127.71, 127.47, 126.98, 124.99, 124.59, 70.29, 30.63, 21.71, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.18 (s, 1H), 6.82 (dd, 2H), 4.48-4.34 (m, 4H), 2.85 (dd, 1H), 1.85 (s, 3H), 0.31 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 149.53, 143.03, 126.95, 123.36, 121.49, 117.25, 110.05, 71.70, 61.57, 31.71, 21.02, −1.62;

¹H NMR (400 MHz, CDCl₃): δ 6.99 (d, 2H), 6.87 (s, 1H), 5.97 (s, 2H), 2.72 (s, 2H), 2.14 (s, 3H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 151.58, 147.84, 132.17, 123.36, 123.13, 111.80, 104.82, 101.95, 71.70, 31.71, 21.02, −2.02;

¹H NMR (400 MHz, CDCl₃): δ 7.40-7.29 (m, 5H), 4.21 (s, 1H), 3.30 (dd, 2H), 2.98 (dd, 2H), 1.70 (m, 2H), 0.23 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 136.86, 131.37, 128.99, 126.52, 108.38, 71.73, 43.63, 28.27, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): δ 7.17 (d, 1H), 5.89 (d, 1H), 5.54 (s, 1H), 5.46 (s, 1H), 3.89 (s, 3H), 2.89 (dd, 2H), 0.27 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 162.06, 133.50, 123.31, 113.36, 112.44, 107.34, 58.24, 52.08, 28.43, −1.76;

¹H NMR (400 MHz, CDCl₃): δ 7.67 (d, 1H), 6.47-6.39 (m, 2H), 2.89 (dd, 2H), 1.88 (s, 3H), 0.23 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 158.66, 142.80, 118.78, 112.07, 105.96, 74.67, 29.37, 21.02, −1.62;

¹H NMR (400 MHz, CDCl₃): δ 6.27-6.03 (m, 2H), 2.83 (dd, 2H), 2.30 (dd, 3H), 1.86 (s, 3H), 0.23 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 158.49, 155.72, 118.78, 109.82, 108.25, 75.26, 29.37, 21.02, 14.79, −1.66;

¹H NMR (400 MHz, CDCl₃): δ 6.57-6.53 (m, 2H), 2.84 (dd, 2H), 2.36 (s, 3H), 1.88 (s, 3H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 142.28, 142.06, 126.40, 120.85, 114.09, 79.52, 30.74, 21.02, 17.13, −1.62;

¹H NMR (400 MHz, CDCl₃): δ 5.57-5.53 (m, 2H), 5.03 (s, 1H), 2.54 (dd, 2H), 2.16 (s, 3H), 1.80 (s, 3H), 0.19 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 139.22, 132.45, 123.36, 106.96, 105.88, 70.68, 30.20, 21.02, 13.43, −1.52;

¹H NMR (400 MHz, CDCl₃): δ 7.95-7.53 (m, 3H), 2.73 (s, 3H), 2.84 (dd, 2H), 2.56 (s, 3H), 1.87 (s, 3H), 0.19 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 160.63, 156.83, 140.70, 124.71, 123.91, 119.14, 69.32, 29.74, 24.29, 21.02, −0.62;

¹H NMR (400 MHz, CDCl₃): 7.32-7.28 (m, 2H), 7.23-7.19 (m, 3H), 2.90-2.78 (m, 4H), 2.08-2.04 (m, 2H), 1.66 (s, 3H), 0.40 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.51, 128.67, 128.43, 126.35, 121.59, 69.92, 45.04, 30.74, 29.81, 29.02, −1.73, −1.82;

¹H NMR (400 MHz, CDCl₃): δ 8.39 (s, 1H), 7.85-7.53 (dd, 2H), 2.84 (dd, 2H), 2.33 (s, 3H), 1.88 (s, 3H), 0.21 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 156.16, 148.39, 132.96, 131.39, 123.91, 117.27, 69.17, 29.74, 21.02, 18.43, −1.62;

¹H NMR (400 MHz, CDCl₃): δ 8.49 (d, 1H), 7.87 (s, 1H), 7.53 (d, 1H), 2.94 (dd, 2H), 2.36 (s, 3H), 1.87 (s, 3H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 157.81, 149.77, 147.81, 125.60, 123.91, 118.49, 68.85, 29.74, 21.23, 21.02, −1.72;

¹H NMR (400 MHz, CDCl₃): δ 4.26 (s, 1H), 2.97 (dd, 2H), 0.94 (s, 9H), 0.23 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 121.84, 73.83, 34.39, 28.43, 27.08, −1.86;

¹H NMR (400 MHz, CDCl₃): δ 4.22 (s, 1H), 2.98 (dd, 2H), 1.85 (q, 2H), 0.90 (t, 3H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 119.12, 64.40, 28.43, 26.00, 10.41, −1.86;

¹H NMR(400 MHz, CDCl₃): δ 4.21 (d, 1H), 2.98 (dd, 2H), 1.90 (m, 2H), 0.90 (d, 6H), 0.22 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 118.35, 69.93, 37.79, 28.43, 18.42, −1.86;

4) Nucleophilic Addition Reaction of Functionalized Silyl Cyanide 1aaa with Imines (Table 4).

General procedure 4: acatalyst I′ (0.1 mmol), imine 3b (1.0 mmol) and a corresponding solvent (1 mL) were added into a dry Schlenk tube (25 mL). The mixture was added with 1aaa (2.0 mmol) after being stirred at the corresponding temperature for 0.5 h. The progress of the reaction was monitored by TLC analysis. After full consumption of the raw material 3b, 4b as shown in Scheme (IIb) was obtained by conventional post-treatment followed by column chromatography, or by column chromatography directly.

The specific experimental operations of the examples 116-159 are referred to general procedure 4. The specific reaction conditions and yields of each example are shown in Table 4.

TABLE 4 Specific reaction conditions and yields of the examples 116-159. Product/ Ex- Temper- Yield am- Catalyst I′ ature (%)/ ple R² R³ PG (ml %) Solvent (° C.) Ee (%) 116 C₆H₅ H Bn

  DMAP (25) CH₃CN 25 4ba/79/— 117 C₆H₅ H CBz DMAP (2.5) toluene 25 4bb/86/— 118 C₆H₅ H Ts DMAP (2.5) CH₂Cl₂ 25 4bc/88/— 119 C₆H₅ H Boc DMAP (2.5) CH₂Cl₂ 25 4bd/93/— 120 C₆H₅ H PMP DMAP (15) CH₃CN 25 4be/82/— 121 C₆H₅ H P(O)Ph₂ DMAP (5) toluene 25 4bf/90/— 122 C₆H₅ H PMP DMAP (15) CH₂Cl₂ 25 4bg/89/— 123 C₆H₅ CONMe₂ PMP DMAP (50) CH₂Cl₂ 25 4bh/86/— 124 C₆H₅ CONEt₂ PMP DMAP (50) THF 50 4bi/88/— 125 C₆H₅ Me PMP KOAc (15) CH₃CN 50 4bj/85/— 126 C₆H₅ CO₂Me PMP KOAc (25) toluene 25 4bk/89/— 127 C₆H₅ CO₂Et PMP K₂CO₃ (25) CH₂Cl₂ 25 4bl/87/— 128 C₆H₅ CO₂t—Bu PMP K₂CO₃ (25) CH₂Cl₂ 50 4bm/78/— 129 C₆H₅ CO₂Bn PMP K₂CO₃ (25) CH₃CN 25 4bn/89/— 130 4-Cl—C₆H₄ H Ts Et₃N (15) THF 40 4bo/87/— 131 3-Cl—C₆H₄ H Ts (i-Pr)₂NEt (25) toluene 50 4bp/83/— 132 2-Cl—C₆H₄ H Ts Et₃N (15) CH₂Cl₂ 55 4bq/87/— 133 4-F—C₆H₄ H Ts Et₃N (15) CH₂Cl₂ 25 4br/85/— 134 4-Br—C₆H₄ H Ts (i-Pr)₂NEt (25) CH₃CN 25 4bs/82/— 135

H Ts

  DABCO (5) toluene 50 4bt/95/— 136

H Ts DMAP (5) CH₂Cl₂ 25 4bu/85/— 137

H Ts DMAP (5) CH₂Cl₂ 50 4bv/80/— 138

H Ts DMAP (5) CH₃CN 25 4bw/89/— 139 Bn H PMP ZnI₂ (0.5) CH₂Cl₂ 0 4bx/82/— 140 BnCH₂ H PMP TiCl₄ (2.5) CH₂Cl₂ 0 4by/87/— 141 Cy H PMP Et₃N (5) CH₂Cl₂ 0 4bz/92/— 142 C₆H₅ H Bn IC3 (20) CH₃CN −20   4ba/83/75 143 C₆H₅ H CBz IC3 (5) toluene −20   4bb/96/90 144 C₆H₅ H Ts IC3 (10) CH₂Cl₂ −20   4bc/89/94 145 C₆H₅ H Boc IC3 (5) CH₂Cl₂ −20   4bd/93/93 146 C₆H₅ H PMP IC3 (10) CH₂Cl₂ −20   4be/86/87 147 C₆H₅ H P(O)Ph₂ IC3 (20) CH₂Cl₂ −20   4bf/80/88 148 4-Cl—C₆H₄ H Ts IC3 (10) CH₂Cl₂ −20   4bo/92/93 149 3-Cl—C₆H₄ H Ts IC3 (10) CH₂Cl₂ −20   4bp/95/84 150 2-Cl—C₆H₄ H Ts IC3 (10) CH₂Cl₂ −20   4bq/87/82 151 4-F—C₆H₄ H Ts IC3 (10) CH₂Cl₂ −20   4br/84/94 152 4-Br—C₆H₄ H Ts IC3 (10) CH₂Cl₂ −20   4bs/86/93 153

H Ts IC3 (10) CH₂Cl₂ −20   4bt/94/95 154

H Ts IC3 (10) CH₂Cl₂ −20   4bu/95/82 155

H Ts IC3 (10) CH₂Cl₂ −20   4bv/90/90 156

H Ts IC3 (10) CH₂Cl₂ −20   4bw/89/91 157 Bn H PMP IC3 (20) CH₂Cl₂ −20   4bx/80/68 158 BnCH₂ H PMP IC3 (20) CH₂Cl₂ −20   4by/90/75 159 Cy H PMP IC3 (20) CH₂Cl₂ −20   4bz/92/90

Products 4ba-4bz are known compounds. The characterizations of the products 4ba, 4be are consistent with the literature (Chem. Comm. 2009, 34, 5180); the characterizations of the products 4bb, 4bd are consistent with the literature (Org. Lett.2012, 14, 882); the characterizations of the products 4bc, 4bj, 4bo, 4br, 4bt, 4bu, 4bw, 4bx, 4bz are consistent with the literature (Angew. Chem. Int. Ed. 2007,46, 8468); the characterization of the product 4bf is consistent with the literature (J. Am. Chem. Soc. 2009, 131, 15118); the characterizations of the products 4bg, 4by are consistent with the literature (Tetrahedron Lett. 2012, 53, 1075); the characterizations of the products 4bh, 4bi, 4bk, 4bl, 4bm, 4bn are consistent with the literature (Angew. Chem. Int. Ed. 2015,54, 13655); the characterizations of the products 4 bp, 4bv are consistent with the literature (Tetrahedron Lett. 2004, 45, 9565); and the characterizations of the products 4bq, 4bs, 4bx are consistent with the literature (Tetrahedron Lett. 2014, 55, 232).

5) Addition Reaction of the Functionalized Silyl Cyanide 1aaa with an Electron-Deficient Olefin (Table 5).

General procedure 5: the catalyst I (0.1 mmol), an electron-deficient olefin 3c (1.0 mmol) and a corresponding solvent (1 mL) were added into a dry Schlenk tube (25 mL). The mixture was added with the 1aaa (2.0 mmol) after being stirred at a corresponding temperature for 0.5 h. The progress of the reaction was monitored by TLC analysis. After the consumption of the raw material 3c was complete, 4c as shown in Scheme (IIc) was obtained by conventional post-treatment followed by column chromatography, or by column chromatography directly.

The specific experimental operations of the examples 160-182 are referred to general procedure 5. The specific reaction conditions and yield of each example are shown in Table 5.

TABLE 5 Specific reaction conditions and yields of the examples 160-182. Product/ Yield Catalyst I Temperature (%)/Ee Example R² R³ EWG (ml %) Solvent (° C.) (%) 160 C₆H₅ H NO₂ DMAP CH₃CN 25 4ca/79/— (25) 161 C₆H₅ H CO₂Me DMAP toluene 25 4cb/86/— (2.5) 162 C₆H₅ H CONMe₂ DMAP CH₃CN 25 4cc/82/— (15) 163 4-Cl—C₆H₄ H NO₂ Et₃N (15) THF 40 4cd/87/— 164 3-NO₂—C₆H₄ H NO₂ (i-Pr)₂NEt toluene 50 4ce/83/— (25) 165 2-Cl—C₆H₄ H NO₂ Et₃N (15) CH₂Cl₂ 55 4cf/87/— 166 4-NO₂—C₆H₄ H NO₂ Et₃N (15) THF 40 4cg/87/— 167 4-OMe—C₆H₄ H NO₂ Et₃N (15) THF 40 4ch/87/— 168 4-F—C₆H₄ H NO₂ Et₃N (15) THF 40 4ci/89/— 169 Cy H NO₂ Et₃N (5) CH₂Cl₂ 0 4cj/92/— 170 Ph Me NO₂ Et₃N (25) CH₂Cl₂ 70 4ck/86/— 171 Ph CF₃ NO₂ Et₃N (25) CH₂Cl₂ 30 4cl/80/— 172 C₆H₅ H NO₂ IC1 toluene −20 4ca/79/85 (R⁴ = OEt) 173 C₆H₅ H CO₂Me IC1 toluene −20 4cb/86/80 (R⁴ = OEt) 174 C₆H₅ H CONMe₂ IC1 toluene −20 4cc/82/68 (R⁴ = OEt) 175 4-Cl—C₆H₄ H NO₂ IC1 THF −20 4cd/87/88 (R⁴ = OEt) 176 3-NO₂—C₆H₄ H NO₂ IC1 toluene −20 4ce/83/87 (R⁴ = OEt) 177 2-Cl—C₆H₄ H NO₂ IC1 CH₂Cl₂ −20 4cf/87/80 (R⁴ = OEt) 178 4-NO₂—C₆H₄ H NO₂ IC1 THF −20 4cg/87/86 (R⁴ = OEt) 179 4-OMe—C₆H₄ H NO₂ IC1 THF −20 4ch/87/88 (R⁴ = OEt) 180 Cy H NO₂ IC1 CH₂Cl₂ −20 4cj/92/87 (R⁴ = OEt) 181 Ph Me NO₂ IC1 CH₂Cl₂ 20 4ck/90/70 (R⁴ = OEt) 182 Ph CF₃ NO₂ IC1 CH₂Cl₂ −20 4cl/80/85 (R⁴ = OEt)

Products 4ca-4c1 are known compounds. The characterizations of the compounds 4ca, 4cd-h are consistent with the literature (Tetrahedron Lett.2009, 50, 640); the characterization of the compound 4cb is consistent with the literature (Org. Biomol. Chem. 2010, 8, 533); the characterization of the compound 4cj is consistent with the literature (Org. Lett. 2008, 10, 4141); the characterization of the compound 4ck is consistent with the literature (Chem. Eur. 12015, 21, 1280); and the characterization of the compound 4c1 is consistent with the literature (RSC Adv. 2016, 6, 29977).

6) Nucleophilic Addition Reaction of Different Functionalized Silyl Cyanide 1a with Ketone 3Aao (Table 6).

General procedure 6: a catalyst IC1 (R⁴=OEt) (0.05 mol), ketone 3aao (1 mmol) and Et₂O (1 mL) were added into a dry Schlenk tube (25 mL). The mixture was added with 1a after being stirred at a corresponding temperature for 0.5 h. The progress of the reaction was monitored by TLC analysis. After the consumption of the raw material 3aao was complete, 4d as shown in Scheme (IId) was obtained by conventional post-treatment followed by column chromatography, or by column chromatography directly, wherein, the compound 4d is in R or S configuration.

The specific experimental operations of the examples 183-199 are referred to general procedure 6. The specific reaction conditions and yield of each example are shown in Table 6.

TABLE 6 Specific reaction conditions and yields of the examples 183-199. Temperature Product/ Example 1a (mmol) (° C.) Yield (%)/Ee (%) 183 1aab (1.0) −30 4da/76/95 184 1aab (1.2) −30 4da/89/95 185 1aab (1.5) −30 4da/95/95 186 1aab (1.75) −30 4da/96/95 187 1aab (2.0) −30 4da/96/95 188 1aab (2.5) −30 4da/97/93 189 1aab (3.0) −30 4da/98/90 190 1aba (1.5) −40 4db/96/93 191 1aea (1.5) 0 4dc/79/85 192 1aeb (1.5) 0 4dd/87/88 193 1abc (1.5) −10 4de/89/94 194 1aec (1.5) 10 4df/91/87 195 1abd (1.5) −20 4dg/96/96 196 1abc (1.5) −40 4dh/89/95 197 1aca (1.5) −20 4di/88/90 198 1ada (1.5) −10 4dj/92/90 199 1adb (1.5) −20 4dk/94/94

The characterizations of 4da-4dk are as follows:

¹H NMR (400 MHz, CDCl₃): 7.42-7.29 (m, 2H), 7.29-7.19 (m, 3H), 2.60-2.48 (m, 4H), 2.08-2.04 (m, 2H), 1.67 (s, 3H), 0.40 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.55, 128.17, 128.33, 126.45, 121.79, 69.82, 45.44, 30.84, 30.91, 29.12, −1.75, −1.86;

¹H NMR (400 MHz, CDCl₃): 7.41-7.30 (m, 2H), 7.26-7.17 (m, 3H), 5.30 (dd, 1H), 5.22-5.17 (m, 2H), 2.55-2.48 (m, 2H), 2.08-2.04 (m, 2H), 1.68 (s, 3H), 0.42 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 143.84, 140.87, 128.91, 128.43, 128.11, 126.57, 119.43, 69.88, 40.92, 33.90, 27.60, −1.78, −1.89;

¹H NMR (400 MHz, CDCl₃): 7.47-7.32 (m, 2H), 7.26-7.17 (m, 3H), 2.81 (s, 1H), 2.55-2.48 (m, 2H), 2.08-2.04 (m, 2H), 1.68 (s, 3H), 0.42 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 128.91, 128.43, 126.57, 119.43, 118.74, 70.41, 51.51, 40.92, 33.90, 27.60, −1.78, −1.89;

¹H NMR (400 MHz, CDCl₃): 7.47-7.32 (m, 2H), 7.26-7.17 (m, 3H), 2.83 (s, 1H), 2.56-2.47 (m, 2H), 2.08-2.04 (m, 4H), 1.70 (s, 3H), 1.25 (t, 2H), 0.42 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 128.91, 128.43, 126.57, 119.43, 84.72, 68.96, 64.57, 40.92, 33.90, 27.60, 18.16, 12.42, −1.78, −1.89;

¹H NMR (400 MHz, CDCl₃): δ 7.49-7.37 (m, 2H), 7.28-7.19 (m, 3H), 5.30 (t, 1H), 2.54 (t, 2H), 2.09 (t, 2H), 2.00 (d, 2H), 1.69 (s, 3H), 1.59 (s, 3H), 1.44 (s, 3H), 0.43 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 128.91, 128.43, 127.89, 126.57, 119.83, 119.43, 68.96, 40.92, 33.90, 27.60, 25.15, 18.07, 14.78, −1.77, −1.88;

¹H NMR (400 MHz, CDCl₃): δ 7.55-7.40 (m, 2H), 7.26-7.17 (m, 3H), 2.54 (t, 2H), 2.09 (t, 2H), 1.80 (s, 3H), 1.69 (s, 3H), 0.42 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 128.91, 128.43, 126.57, 119.43, 103.01, 79.50, 70.41, 40.92, 33.90, 27.60, 7.11, −1.78, −1.89;

¹H NMR (400 MHz, CDCl₃): 7.41-7.30 (m, 2H), 7.26-7.17 (m, 3H), 5.97-5.80 (m, 1H), 5.17-5.19 (m, 2H), 2.57 (t, 2H), 2.49-2.15 (m, 4H), 1.81 (m, 2H), 1.39-1.25 (m, 4H), 1.15-1.08 (m, 2H), 0.43 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 138.80, 128.91, 128.43, 126.57, 119.43, 114.45, 68.96, 40.92, 35.17, 33.90, 29.94, 27.60, 23.57, 15.78, −1.77, −1.88;

¹H NMR (400 MHz, CDCl₃): 7.41-7.30 (m, 2H), 7.26-7.17 (m, 3H), 5.70 (dd, 1H), 5.12-5.07 (m, 2H), 2.55-2.48 (m, 2H), 2.08-2.04 (m, 4H), 1.69 (s, 3H), 0.43 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 135.46, 128.91, 128.43, 126.57, 119.43, 110.94, 68.96, 40.92, 33.90, 27.60, 23.11, −1.77, −1.88;

¹H NMR (400 MHz, CDCl₃): 7.43-7.33 (m, 2H), 7.29-7.18 (m, 3H), 5.70 (s, 1H), 2.58-2.48 (m, 2H), 2.08-2.04 (m, 2H), 1.75 (s, 3H), 0.49 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 128.91, 128.43, 126.57, 119.43, 69.17, 40.92, 33.90, 27.86, 17.56, −1.77, −1.88;

¹H NMR (400 MHz, CDCl₃): 7.42-7.29 (m, 2H), 7.29-7.19 (m, 3H), 5.30-5.17 (m, 1H), 2.54 (t, 4H), 2.08 (t, 2H), 1.69 (s, 3H), 1.48-1.40 (m, 2H), 0.43 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 128.91, 128.43, 126.57, 119.43, 68.96, 50.36, 40.92, 33.90, 27.60, −1.75, −1.86;

¹H NMR (400 MHz, CDCl₃): 7.43-7.30 (m, 2H), 7.24-7.15 (m, 3H), 5.40 (t, 1H), 2.55 (t, 4H), 2.07 (t, 2H), 1.69 (s, 3H), 1.58 (d, 2H), 0.44 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 140.87, 128.91, 128.43, 126.57, 119.43, 92.42, 69.76, 68.96, 40.92, 33.90, 27.60, −1.75, −1.86.

7) Tandem Nucleophilic Addition Reaction/Functional Group Transfer Reaction of the Functionalized Silyl Cyanide 1aa (Table 7)

General procedure 7: the catalyst I, the raw material of 3a (1.0 mmol) and a corresponding solvent (1 mL) were added into a dry Schlenk tube (25 mL). The mixture was added with 1aa (1.5 mmol) after being stirred at a T₁ temperature for 0.5 h. The progress of the reaction was monitored by TLC analysis. After the consumption of the raw material 3a was complete, the crude product 4a was obtained by filtering the reaction mixture by 5 cm silica gel column, eluting with Et₂O, and removing solvent under reduced pressure. The crude product 4a was transferred to a dry Schlenk tube (25 mL) and dissolved with anhydrous THF (4.0 mL). The resulting solution was stirred at a T₂ temperature for 0.5 h, and base I was added dropwise slowly. The process of the reaction was monitored by TLC analysis. After the consumption of 4a was complete, the reaction was quenched by 5 mL acid I (4 M). The resulting mixture was extracted three times with EtOAc. Product 5 as shown in Scheme (III) was obtained by rotary evaporation of the solvent and column chromatography.

The specific experimental operations of the examples 200-241 are referred to general procedure 7. The specific reaction conditions and yield of each example are shown in Table 7.

TABLE 7 Specific reaction conditions and yields of the examples 200-241. Ex- Catalyst Product/ am- I T₁ Base I (eq) Yield (%)/ ple R²/R³/Z (mol %) Solvent (° C.) T₂ (° C.) Acid I Ee (%) 200 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/68/— (1.2) −30 acid 201 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/80/— (1.5) −30 acid 202 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/78/— (2.0) −30 acid 203 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/75/— (3.0) −30 acid 204 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/65/— (1.5) −30 acid 205 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Sulfuric 5a/78/— (1.5) −30 acid 206 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 NaHMDS Hydrochloric 5a/38/— (1.5) −30 acid 207 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/66/— (1.5) −78 acid 208 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/75/— (1.5) −50 acid 209 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/68— (1.5) 0 acid 210 BnCH₂/Me/Cl Na₂CO₃ (5) MeCN 25 LDA Hydrochloric 5a/39/— (1.5) 30 acid 211 BnCH₂/Et/Cl K₂CO₃ (5) MeCN 25 LDA Hydrochloric 5b/78/— (1.5) −30 acid 212 BnCH₂/i-Pr/Cl K₂CO₃ (5) MeCN 50 LDA Hydrochloric 5c/74/— (1.5) −30 acid 213

KOAc (25) MeCN 25 LDA (1.5) −30 Hydrochloric acid 5d/68/— 214

K₂CO₃ (15) THF 25 LDA (1.5) −30 Hydrochloric acid 5e/57/— 215 4-Cl—C₆H₄/Me/Cl Et₃N (5) THF 40 LDA Hydrochloric 5f/64/— (1.5) −30 acid 216 4-Me—C₆H₄/Me/Cl K₂CO₃ (25) THF 0 LDA Hydrochloric 5g/75/— (1.5) −30 acid 217

DABCO (5) THF 50 LDA (1.5) −30 Hydrochloric acid 5h/69/— 218

DMAP (10) MeCN 25 LDA (1.5) −30 Hydrochloric acid 5i/67/— 219

KI (10) MeCN 25 LDA (1.5) −30 Hydrochloric acid 5j/75/— 220

TiCl₄ (0.5) toluene 0 LDA (1.5) −30 Hydrochloric acid 5k/58/— 221

ZnI₂ (0.5) MeCN 25 LDA (1.5) −30 Hydrochloric acid 5l/60/— 222 Et/Me/Cl Zn(OTf)₂ (1) toluene 25 LDA Hydrochloric 5m/68/— (1.5) −30 acid 223 i-Pr/Me/Cl Zn(OTf)₂ (1) toluene 25 LDA Hydrochloric 5n/66/— (1.5) −30 acid 224 CyCH₂/Et/Cl Zn(OTf)₂ (0.1) MeCN 25 LDA Hydrochloric 5o/70/— (1.5) −30 acid 225 CyCH₂/Allyl/Cl K₂CO₃ (1) MeCN 50 LDA Hydrochloric 5p/48/— (1.5) −30 acid 226 BnCH₂/Me/Cl IC1 (10) (R⁴ = OEt) Et₂O 25 LDA Hydrochloric 5a/68/95 (1.5) −30 acid 227 BnCH₂/Et/Cl IC1 (10) (R⁴ = OEt) MeCN 25 LDA Hydrochloric 5b/64/89 (1.5) −30 acid 228 BnCH₂/i-Pr/Cl IC1 (10) (R⁴ = OEt) MeCN 50 LDA Hydrochloric 5c/58/78 (1.5) −30 acid 229

IC1 (10) (R⁴ = OEt) Et₂O 25 LDA (1.5) −30 Hydrochloric acid 5d/62/85 230

IC1 (20) (R⁴ = OEt) THF 25 LDA (1.5) −30 Hydrochloric acid 5e/58/87 231 4-Cl—C₆H₄/Me/Cl IC1 (10) (R⁴ = OEt) THF 40 LDA Hydrochloric 5f/65/94 (1.5) −30 acid 232 4-Me—C₆H₄/Me/Cl IC4 (20) THF 0 LDA Hydrochloric 5g/59/90 (1.5) −30 acid 233

IC1 (10) (R⁴ = OEt) THF 50 LDA (1.5) −30 Hydrochloric acid 5h/68/90 234

IC1 (10) (R⁴ = OEt) MeCN 25 LDA (1.5) −30 Hydrochloric acid 5i/72/89 235

IC1 (10) (R⁴ = OEt) CH₂Cl₂ 25 LDA (1.5) −30 Hydrochloric acid 5j/70/90 236

IC1 (10) (R⁴ = OEt) toluene 0 LDA (1.5) −30 Hydrochloric acid 5k/60/86 237

IC2 (10) (X¹ = NTf₂) MeCN 25 LDA (1.5) −30 Hydrochloric acid 5l/58/80 238 Et/Me/Cl IC1 (10) (R⁴ = OEt) Et₂O 25 LDA Hydrochloric 5m/70/90 (1.5) −30 acid 239 i-Pr/Me/Cl IC1 (10) (R⁴ = OEt) Et₂O 25 LDA Hydrochloric 5n/66/94 (1.5) −30 acid 240 CyCH₂/Et/Cl IC1 (10) (R⁴ = OEt) Et₂O 50 LDA Hydrochloric 5o/65/85 (1.5) −30 acid 241 Cy/Allyl/Cl IC1 (10) (R⁴ = OEt) Et₂O 25 LDA Hydrochloric 5p/58/95 (1.5) −30 acid

The characterizations of 5a-5p are as follows:

¹H NMR (400 MHz, CDCl₃): 7.30-7.27 (m, 2H), 7.22-7.14 (m, 3H), 4.42 (dd, 1H), 4.39 (dd, 1H), 3.10 (s, br, 1H), 2.76-2.73 (m, 1H), 2.48-2.47 (m, 1H), 2.09-2.03 (m, 2H), 1.45 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 205.88, 140.88, 128.67, 128.43, 126.34, 79.43, 45.48, 41.90, 29.83, 26.16;

¹H NMR (400 MHz, CDCl₃): 7.32-7.26 (m, 2H), 7.20-7.13 (m, 3H), 4.42 (dd, 1H), 4.39 (dd, 1H), 3.10 (s, br, 1H), 2.78-2.75 (m, 1H), 2.48-2.47 (m, 1H), 1.83 (q, 2H), 0.95 (t, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 205.88, 140.88, 128.67, 128.43, 126.34, 79.43, 45.48, 41.90, 29.83, 26.16;

¹H NMR (400 MHz, CDCl₃): 7.33-7.25 (m, 2H), 7.21-7.14 (m, 3H), 4.42 (dd, 1H), 4.39 (dd, 1H), 3.14 (s, br, 1H), 2.78-2.75 (m, 1H), 2.48-2.47 (m, 1H), 1.89-1.81 (q, 1H), 0.95 (d, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 213.54, 140.87, 128.91, 128.43, 126.57, 85.61, 46.74, 33.13, 30.70, 27.81, 16.69;

¹H NMR (400 MHz, CDCl₃): 7.33-7.25 (m, 2H), 7.21-7.14 (m, 3H), 5.92 (dd, 1H), 5.30-5.05 (m, 1H), 4.42 (dd, 1H), 4.39 (dd, 1H), 3.16 (s, br, 1H), 2.78-2.75 (m, 1H), 2.48-2.47 (m, 1H); ¹³C NMR (100 MHz, CDCl₃): δ 207.22, 143.05, 140.87, 128.91, 128.43, 126.57, 118.08, 77.54, 46.08, 35.61, 32.84;

¹H NMR (400 MHz, CDCl₃): 7.32-7.24 (m, 2H), 7.21-7.14 (m, 3H), 4.42 (dd, 1H), 4.39 (dd, 1H), 3.17 (s, br, 1H), 2.68-2.60 (m, 1H), 2.48-2.47 (m, 1H), 1.80 (s, 1H); ¹³C NMR (100 MHz, CDCl₃): δ 213.74, 140.87, 128.91, 128.43, 126.57, 75.70, 73.78, 69.54, 45.36, 39.10, 33.22, 7.30;

¹H NMR (400 MHz, CDCl₃): 7.38 (m, 4H), 4.40 (dd, 1H), 4.32 (dd, 1H), 3.56 (s, br, 1H), 1.78 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 202.91, 139.26, 134.61, 129.13, 126.89, 80.16, 45.18, 26.14;

¹H NMR (400 MHz, CDCl₃): 7.30-7.05 (m, 4H), 4.30 (dd, 1H), 4.22 (dd, 1H), 3.36 (s, br, 1H), 2.34 (s, 3H), 1.78 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 202.91, 139.26, 134.61, 129.13, 126.89, 80.16, 45.18, 26.14;

¹H NMR (400 MHz, CDCl₃): 8.10-7.95 (m, 2H), 7.65-7.55 (m, 2H), 7.45 (s, 1H), 7.30 (d, 1H), 4.32 (dd, 1H), 4.25 (dd, 1H), 3.38 (s, br, 1H), 1.88 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 205.09, 146.27, 134.44, 134.11, 130.55, 129.46, 127.57 (d, J=6.1 Hz), 126.56 (d, J=18.2 Hz), 125.97, 79.45, 45.05, 24.85;

¹H NMR (400 MHz, CDCl₃): 7.05 (s, 1H), 6.55 (s, 1H), 4.55 (s, 2H), 4.30 (s, 2H), 4.12 (dd, 1H), 4.05 (dd, 1H), 3.38 (s, br, 1H), 1.88 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 205.09, 147.89, 142.43, 128.97, 122.55, 121.74, 112.84, 79.08, 61.57, 45.05, 24.85;

¹H NMR (400 MHz, CDCl₃): 7.03 (s, 1H), 6.85 (s, 1H), 6.30 (s, 2H), 4.12 (dd, 1H), 4.05 (dd, 1H), 3.58 (s, br, 1H), 1.89 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 205.09, 148.50, 146.18, 135.49, 123.04, 116.17, 107.96, 101.95, 79.08, 45.05, 24.85;

¹H NMR (400 MHz, CDCl₃): 7.63 (d, 1H), 6.55 (dd, 1H), 6.39 (d, 1H), 4.10 (dd, 1H), 4.00 (dd, 1H), 3.54 (s, br, 1H), 1.69 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 214.78, 158.50, 142.80, 112.07, 105.50, 75.98, 45.28, 23.37;

¹H NMR (400 MHz, CDCl₃): 6.35 (d, 1H), 6.09 (dd, 1H), 4.10 (dd, 1H), 4.00 (dd, 1H), 3.54 (s, br, 1H), 1.69 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 214.78, 155.72, 150.21, 111.01, 108.25, 75.10, 45.28, 23.37, 14.79;

¹H NMR (400 MHz, CDCl₃): 4.45 (dd, 2H), 2.97 (s, br, 1H), 1.81-1.67 (m, 2H), 1.39 (s, 3H), 0.86 (t, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 206.00, 79.86, 45.73, 33.02, 25.44, 7.71;

¹H NMR (400 MHz, CDCl₃): 4.47 (dd, 1H), 4.43 (dd, 1H), 2.90 (s, br, 1H), 1.99-1.92 (m, 1H), 1.33 (s, 3H), 0.96 (dd, 1.2 Hz, 3H), 0.79 (d, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 206.56, 81.69, 46.13, 35.49, 23.70, 17.08, 15.86;

¹H NMR (400 MHz, CDCl₃): 4.43 (dd, 1H), 4.37 (dd, 1H), 3.12 (s, br, 1H), 1.72-1.56 (m, 8H), 1.50-1.47 (m, 1H), 1.39-1.32 (m, 1H), 1.25-1.06 (m, 3H), 1.11-0.86 (m, 2H), 0.81 (t, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 206.36, 82.67, 46.64, 46.06, 34.94, 34.39, 33.53, 33.36, 26.29, 26.27, 26.13, 7.49;

¹H NMR (400 MHz, CDCl₃): 5.73-5.66 (m, 1H), 5.19-5.13 (m, 2H), 4.43 (s, 2H), 3.02 (s, 1H), 2.50-2.40 (m, 2H), 1.76-1.60 (m, 6H), 1.54-1.50 (m, 1H), 1.43-1.36 (m, 1H), 1.28-1.08 (m, 3H), 1.01-0.83 (m, 2H); ¹³C NMR (100 MHz, CDCl₃): δ 205.83, 131.52, 120.41, 82.10, 46.80, 46.55, 44.77, 34.88, 34.39, 34.47, 26.29, 26.26, 26.13.

8) Total Synthesis of the Colorado Potato Beetle Aggregation Pheromone (Table 8).

General procedure 8: the catalyst IC1 (R is OEt), ketone 6 (40.0 mmol) and a corresponding solvent (40 mL) were added into a dry Schlenk tube (25 mL). After being stirred at −30° C. for 0.5 h, 1aa (60 mmol) was added to the mixture. The process of the reaction was monitored by TLC analysis. After the consumption of the raw material 6 was complete, crude product 7 was obtained by filtering the reaction mixture by 5 cm silica gel column, eluting with Et₂O, and removing the solvent under reduced pressure. Then the crude product 7 was transferred to a dry Schlenk tube (150 mL) and dissolved with anhydrous THF (40 mL). The mixture was stirred at −30° C. for 0.5 h, and then base LDA (60 mmol) was added dropwise slowly. The process of the reaction was monitored by TLC analysis. After the consumption of the raw material 7 was complete, the reaction mixture was quenched by 20 mL hydrochloric acid (4 M), and extracted three times by EtOAc. Crude 8 was obtained by combing the organic phase, and rotary evaporation of the solvent and dried under vacuum.

Then, the crude 8 was dissolved with tetrahydrofuran (40 mL), and then added KOAc (45 mmol). The mixture was refluxed at 100° C. and the process of the reaction was monitored by TLC analysis. After the 8 was converted completely, the reaction mixture was rotary evaporated to remove the solvent. Then saturated ammonium chloride (40 mL) and ethyl acetate (60 mL) was added for liquid separation, After phase separation, the aqueous phase was extracted with ethyl acetate (40 mL*2). The organic phase combined, dried with anhydrous sodium sulfate and rotary evaporated to remove the solvent to provide light brown oily liquid.

Next, the light brown oily liquid was dissolved in methanol (40 mL), and added K₂CO₃ (45 mmol) while stirring. The resulting solution was heated to reflux at 100° C. oil bath until the corresponding intermediate was converted completely by TLC analysis. The reaction mixture was then rotary evaporated to remove MeOH under reduced pressure. Saturated ammonium chloride (40 mL) and ethyl acetate (60 mL) were added. After phase separation, the aqueous phase was extracted with ethyl acetate (20 mL*2). The organic phase was combined and dried with anhydrous sodium sulfate. After rotary evaporation of the solvent, the resulted light brown oily liquid was subjected to column chromatography to afford pure(S)—CPB as shown in (IV).

The specific experimental operations of the examples 242-243 are referred to general procedure 8. The specific reaction conditions and yield of each example are shown in Table 8.

TABLE 8 Specific reaction conditions and yields of the example 242-243. Example Z Yield (%) Ee (%) 242 Cl 65 97 243 Br 53 96

The characterization of(S)—CPB is as follows:

¹H NMR (400 MHz, CDCl₃): 5.04 (t, 1H), 4.54-4.43 (m, 2H), 2.94 (s, br, 2H), 2.14-2.05 (m, 1H), 1.95-1.87 (m, 1H), 1.83-1.71 (m, 2H), 1.67 (s, 3H), 1.58 (s, 3H), 1.37 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 214.25, 133.39, 123.07, 78.58, 64.76, 40.03, 26.20, 25.71, 22.26, 17.76;

9) Tandem Cyanosilylation Reaction/Ring-Closing Olefin Metathesis of Cyansilane Lab (Table 9).

General procedure 9: the catalyst I (0.05 mmol), a raw material 9 (1.0 mmol) and a corresponding solvent (1 mL) were added into a dry Schlenk tube (25 mL). The mixture was added with 1ab (1.5 mmol) after being stirred at a corresponding temperature for 0.5 h. The progress of the reaction was monitored by TLC analysis. After the consumption of the raw material 9 was complete, crude product 10 was obtained by filtering the reaction mixture by 5 cm silica gel column, eluting with Et₂O, and removing solvent under reduced pressure. The crude product 10 was transferred to a dry Schlenk tube (25 mL) and dissolved with anhydrous CH₂C12 (2.0 mL), and added with catalyst Grubbs I (0.01 mmol) at 25° C. The progress of the reaction was monitored by TLC analysis. After the consumption of the 10 was complete, the desired product11 as shown in Scheme (V) was obtained from the reaction mixture by column chromatography directly.

The specific experimental operations of the examples 244-255 are shown in general procedure 9. The specific reaction conditions and yield of each example are shown in Table 9.

TABLE 9 Specific reaction conditions and yields of the examples 244-255. Example n R⁶ Catalyst I Product Yield (%)/Ee (%) 244 0 Me K₂CO₃ 11a 75/— 245 1 Me K₂CO₃ 11b 73/— 246 4 Me K₂CO₃ 11c 69/— 247 1 H K₂CO₃ 11b 60/— 248 1 Et K₂CO₃ 11b 70/— 249 1 Ph K₂CO₃ 11b 78/— 250 0 Me IC1 11a 68/96 (R⁴ = OEt) 251 1 Me IC1 11b 70/95 (R⁴ = OEt) 252 4 Me IC1 11c 75/92 (R⁴ = OEt) 253 1 H IC1 11b 60/90 (R⁴ = OEt) 254 1 Et IC1 11b 77/96 (R⁴ = OEt) 255 1 Ph IC1 11b 73/92 (R⁴ = OEt)

The characterizations of 11a-11c are as follows:

¹H NMR (400 MHz, CDCl₃): 5.84 (d, 1H), 5.43 (d, 1H), 1.81 (s, 3H), 0.35 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 152.92, 134.94, 117.46, 81.92, 27.70, 2.22;

¹H NMR (400 MHz, CDCl₃): 5.68-5.61 (m, 2H), 2.03 (d, 2H), 1.87 (s, 3H), 0.33 (s, 6H); (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 152.04, 136.84, 118.40, 81.92, 75.78, 27.40, 2.82;

¹H NMR (400 MHz, CDCl₃): 5.67-5.60 (m, 2H), 2.03 (m, 2H), 1.87 (s, 3H), 1.44-1.30 (m, 6H), 0.35 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 137.26, 131.80, 119.50, 75.58, 30.97, 30.00, 29.38, 23.57, 15.78, 2.48.

10) Epoxy Ring-Opening Reaction/Functional Mass Transfer Reaction of Functionalized Silyl Cyanide 1aa (Table 10).

General procedure 10: the catalyst I, a raw material 12 (1.0 mmol) and a corresponding solvent (1 mL) were added into a dry Schlenk tube (25 mL). The mixture was added with 1aa (1.5 mmol) after being stirred at a corresponding temperature for 0.5 h. The process of the reaction was monitored by TLC analysis. After the consumption of the raw material 12 was complete, crude product 13 was obtained by filtering the reaction mixture by 5 cm silica gel column, eluting with Et2O, and removing solvent under reduced pressure. The crude product 13 was transferred to a dry Schlenk tube (25 mL) and dissolved with anhydrous THF (4.0 mL). The resulting solution was stirred at −30° C. for 0.5 h, and then LDA (1.5 mmol) was added dropwise slowly. The progress of the reaction was monitored by TLC analysis. After the consumption of the 13 was complete, the reaction mixture was quenched by 5 mL hydrochloric acid (4 M), and then extracted three times by EtOAc. The desired product 14 as shown in Scheme (III) was obtained by combing the organic phase, rotary evaporating to remove the solvent and column chromatography.

The specific experimental operations of the examples 256-286 are referred to general procedure 10. The specific reaction conditions and yield of each example are shown in Table 10.

TABLE 10 Specific reaction conditions and yields of the examples 256-286 Product/Yield Example R⁷/R⁸/R⁹/Z Catalyst I (mol %) Solvent T1 (° C.) (%)/Ee (%) 256 Ph/Me/Me/ Na₂CO₃ (5) MeCN 25 14a/63/— Cl 257 Ph/Me/Me/ Li₂CO₃ (5) MeCN 25 14a/64/— Cl 258 Ph/Me/Me/ Na₂CO₃ (5) MeCN 25 14a/70/— Cl 259 Ph/Me/Me/ CsOAc (25) MeCN 25 14a/63/— Cl 260 Ph/Me/Me/ Et₃N (5) MeCN 25 14a/68/— Cl 261 Ph/Me/Me/ Zn(OTf)₂ (0.1) MeCN 25 14a/73/— Cl 262 Ph/Me/Me/ KI (10) MeCN 25 14a/66/— Cl 263 Ph/Me/Me/ TiCl₄ (0.5) MeCN 25 14a/65/— Cl 264 Ph/Me/Me/ ZnI₂ (0.5) MeCN 25 14a/65/— Cl 265 Bn/Me/Me/ Na₂CO₃ (5) MeCN 25 14b/71/— Cl 266 BnCH₂/Me/ Na₂CO₃ (5) MeCN 25 14c/75/— Cl 267 BnCH₂/Me/ Na₂CO₃ (5) MeCN 25 14d/65/— Br 268 Et/allyl/allyl/ Na₂CO₃ (5) MeCN 25 14e/65/— Cl 269 Ph/Et/Et/Cl Na₂CO₃ (5) MeCN 40 14f/68/— 270 Ph/Allyl/Allyl/ Na₂CO₃ (5) MeCN 35 14g/66/— Cl 271 Ph/H/H/Cl Na₂CO₃ (5) MeCN 25 14h/38/— 272 Ph/Et/Me/Cl Na₂CO₃ (5) MeCN 25 14i/33/— 273 Ph/Allyl/Me/ Na₂CO₃ (5) MeCN 25 14j/35/— Cl 274 Ph/Me/Me/ IC1 (R⁴ = Me) Et₂O 25 14a/33/87 Cl 275 Ph/Me/Me/ IC1 (R⁴ = OEt) Et₂O −30 14a/40/92 Cl 276 Ph/Me/Me/ IC1 (R⁴ = H) Et₂O −30 14a/31/85 Cl 277 Ph/Me/Me/ IC1 (R⁴ = Ot-Bu) Et₂O −30 14a/37/90 Cl 278 Bn/Me/Me/ IC1 (R⁴ = OEt) Et₂O −30 14b/38/85 Cl 279 BnCH₂/Me/ IC1 (R⁴ = OEt) Et₂O −30 14c/42/80 Cl 280 BnCH₂/Me/ IC1 (R⁴ = OEt) Et₂O −30 14d/35/82 Br 281 Et/allyl/allyl/ IC1 (R⁴ = OEt) Et₂O −30 14e/35/75 Cl 282 Ph/Et/Et/Cl IC1 (R⁴ = OEt) Et₂O −30 14f/35/73 283 Ph/Allyl/Allyl/ IC1 (R⁴ = OEt) Et₂O −30 14g/36/70 Cl 284 Ph/H/H/Cl IC1 (R⁴ = OEt) Et₂O −30 14h/28/67 285 Ph/Et/Me/Cl IC1 (R⁴ = OEt) Et₂O −30 14i/39/80 286 Ph/Allyl/Me/ IC1 (R⁴ = OEt) Et₂O −30 14j/38/85 Cl

The characterizations of compounds 14a-14j are as follows:

¹H NMR (400 MHz, CDCl₃): 7.50-7.38 (m, 2H), 7.22-7.14 (m, 3H), 4.42 (dd, 2H), 3.7 (s, 1H), 3.12 (s, br, 1H), 1.67 (s, 3H), 1.26 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 197.94, 139.14, 131.28, 128.97, 127.91, 74.88, 70.58, 50.52, 26.81;

¹H NMR (400 MHz, CDCl₃): 7.40-7.35 (m, 2H), 7.29-7.17 (m, 3H), 4.52 (dd, 2H), 3.12 (s, br, 1H), 3.09 (dd, 1H), 2.84-2.80 (m, 2H), 1.67 (s, 3H), 1.26 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 202.81, 137.81, 129.07, 128.73, 127.06, 75.93, 63.52, 49.53, 28.58, 27.87;

¹H NMR (400 MHz, CDCl₃): 7.42-7.30 (m, 2H), 7.28-7.15 (m, 3H), 4.54 (dd, 2H), 3.15 (s, br, 1H), 2.55 (t, 2H), 2.40 (t, 1H), 1.86 (1, 2H), 1.67 (s, 3H), 1.25 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 207.26, 141.62, 129.07, 128.37, 126.35, 76.10, 57.27, 49.53, 35.95, 28.58, 25.75;

¹H NMR (400 MHz, CDCl₃): 7.44-7.31 (m, 2H), 7.27-7.14 (m, 3H), 4.46 (dd, 2H), 3.18 (s, br, 1H), 2.56 (t, 2H), 2.43 (t, 1H), 1.85 (1, 2H), 1.67 (s, 3H), 1.27 (s, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 206.07, 141.62, 129.07, 128.37, 126.35, 76.10, 60.50, 38.06, 35.95, 28.58, 25.75;

¹H NMR (400 MHz, CDCl₃): 5.94-5.81 (m, 2H), 5.17-4.94 (m, 4H), 4.47 (dd, 2H), 3.58 (s, br, 1H), 2.58 (q, 1H), 2.13 (d, 2H), 1.67 (s, 3H), 1.15 (d, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 198.64, 133.18, 119.40, 73.02, 52.25, 48.49, 47.30, 10.56;

¹H NMR (400 MHz, CDCl₃): 7.47-7.39 (m, 2H), 7.32-7.14 (m, 3H), 4.41 (dd, 2H), 3.73 (s, 1H), 3.15 (s, br, 1H), 1.67 (s, 3H), 1.55 (q, 4H), 0.96 (t, 6H); ¹³C NMR (100 MHz, CDCl₃): δ 198.74, 138.38, 131.51, 128.96, 127.79, 72.56, 65.98, 50.52, 31.54, 7.62;

¹H NMR (400 MHz, CDCl₃): 7.47-7.39 (m, 2H), 7.32-7.14 (m, 3H), 5.94-5.81 (m, 2H), 5.17-4.94 (m, 4H), 4.42 (dd, 2H), 3.73 (s, 1H), 3.15 (s, br, 1H), 2.05 (d, 4H), 1.67 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 198.74, 138.38, 133.18, 131.51, 128.96, 127.79, 119.40, 72.78, 69.84, 50.52, 44.59;

¹H NMR (400 MHz, CDCl₃): 7.45-7.33 (m, 2H), 7.27-7.14 (m, 3H), 4.45 (dd, 2H), 4.23 (dd, 1H), 3.95 (dd, 1H), 3.65 (s, br, 1H), 1.67 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 189.78, 137.59, 130.52, 128.69, 128.24, 66.24, 55.33, 51.14;

¹H NMR (400 MHz, CDCl₃): 7.46-7.38 (m, 2H), 7.33-7.15 (m, 3H), 4.41 (dd, 2H), 3.74 (s, 1H), 3.45 (s, br, 1H), 1.67 (s, 3H), 1.53 (q, 2H), 1.23 (s, 3H), 0.95 (t, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 199.25, 138.12, 131.06, 128.93, 127.66, 72.93, 65.48, 50.52, 33.39, 23.22, 7.41;

¹H NMR (400 MHz, CDCl₃): 7.47-7.39 (m, 2H), 7.32-7.14 (m, 3H), 5.90-5.80 (m, 1H), 5.19-4.92 (m, 2H), 4.45 (dd, 2H), 3.75 (s, 1H), 3.35 (s, br, 1H), 2.05 (dd, 1H); 1.95 (dd, 1H), 1.67 (s, 3H), 1.36 (s, 3H); ¹³C NMR (100 MHz, CDCl₃): δ 199.25, 138.12, 133.16, 131.06, 128.93, 127.66, 119.35, 74.20, 68.20, 50.52, 45.79, 24.04.

It will be apparent to those skilled in the art that modifications and variations can be made without departing from the scope and spirit disclosed by the appended claims of the present disclosure, and such modifications and variations all fall in the protection extent of the claims of the present disclosure. 

What is claimed is:
 1. A functionalized silyl cyanide having the following formula (1):

wherein, FG is selected from F, Cl, Br, I, CHF₂, CHCl₂, —CH₂CH═CR₂, —CH═CR₂ and —C≡CR; wherein, —CH₂CH═CR₂, —CH═CR₂ and —CCR are functional groups having unsaturated carbon-carbon bond, wherein, R is H, Me; R¹ is Me, Et; n=1-5.
 2. A method for synthesizing functionalized silyl cyanide, comprising the step of: reacting a raw material silane compound 2 and a cyanide source MCN using a metal salt NX¹ _(a) as the catalyst, in an organic solvent, thereby producing the functionalized silyl cyanide 1; the method is as shown in Scheme (I):

wherein; FG is selected from F, Cl, Br, I, CHF₂, CHCl₂, —CH₂CH═CR₂, —CH═CR₂, and —CCR; wherein, —CH₂CH═CR₂, —CH═CR₂ and —CCR are functional groups having unsaturated carbon-carbon bond; wherein, R is H, Me; R¹ is Me, Et; X is selected from Cl, Br, I, and OTf; n=1-5; MCN is HCN or inorganic cyanide, wherein, M=H, Li, Na, K; NX¹ _(a) is inorganic salt, wherein, N═Li, Na, K, Mg, Zn, X¹═Br, I, OTf, a=1-3; the organic solvent is one or more of N,N-dimethylformamide, N,N-dimethylacetamide, dimethyl sulfoxide, tetrahydrofuran, acetonitrile, dichloromethane, and toluene; the molar ratio of silane compound 2, MCN and NX¹ _(a) is 100-300: 150-300: 3-9.
 3. Use of a functionalized silyl cyanide for nucleophilic addition reaction, comprising the steps of: reacting a functionalized silyl cyanide 1a and electrophilic reagent 3 under the catalysis of a catalyst I, to synthesize a compound 4 by nucleophilic addition reaction; wherein, the nucleophilic addition reaction comprises racemic nucleophilic addition reaction and asymmetric nucleophilic addition reaction; the compound 4 is in R and/or S configuration; the process of the reaction is as shown in Scheme (II):

wherein, FG is selected from F, Cl, Br, I, CHF₂, CHCl₂, —CH₂CH═CR₂, —CH═CR₂, and —C≡CR; wherein, —CH₂CH═CR₂, —CH═CR₂ and —C≡CR are functional groups having unsaturated carbon-carbon bond; wherein, R is H, Me; n=1-5; R² is selected from C1-C20 alkyl, phenyl, C6-C20 substituted phenyl, naphthyl, C10-C20 substituted naphthyl, furanyl, C4-C10 substituted furanyl, thienyl, C4-C10 substituted thienyl, pyrryl, C4-C10 substituted pyrryl, pyridyl, and C5-C10 substituted pyridyl; Y is selected from O, NBn, NCbz, NTs, NBoc, NPMP, NP(O)Ph₂, and CHEWG; wherein, EWG ═CN, NO₂, CO₂R, CONR₂, wherein, R=Me, Et, Ph, Bn; R³ is selected from H; C1-C20 alkyl; ester group CO₂R, wherein, R=Me, Et, i-Pr, t-Bu, Ph, Bn; and amide CONR₂, wherein, R=Me, Et, CF₃; R⁵ is H or silyl; when the substrates are not the same, the corresponding products are different; the catalyst I is used for catalyzing the nucleophilic addition reaction of the functionalized silyl cyanide 1a to the electrophilic reagent 3; and the dosage of the catalyst I is 0.001-0.5 equivalent relative to the electrophilic reagent 3; the racemic nucleophilic addition reaction and the asymmetric nucleophilic addition reaction differ in that, the catalysts are not the same, with the other reaction conditions are the same: for the racemic nucleophilic addition reaction, the catalyst I′ comprises: 1) achiral inorganic Lewis base catalyst, comprising: inorganic metal carbonate, carboxylate and phosphate; wherein, the inorganic metal carbonate comprises K₂CO₃, Li₂CO₃, Na₂CO₃, and Cs₂CO₃; the carboxylate comprises KOAc, LiOAc, NaOAc, and CsOAc; and the phosphate comprises K₃PO₄, Li₃PO₄, and Na₃PO₄; 2) achiral organic Lewis base catalyst, comprising: tertiary amine compounds comprising Et₃N, DABCO, and i-Pr₂NEt; piperidine, pyridine derivatives comprising DMAP, N-methyl piperidine, oxynitride

3) achiral Lewis acid catalyst, comprising metal salt comprising ZnI₂, KI, Zn(OTf)₂, and TiCl₄; for the asymmetric nucleophilic addition reaction, the catalyst I″ comprises: chiral Lewis acid catalyst, chiral Lewis base catalyst and chiral bifunctional catalyst having both Lewis acid functional group and Lewis base functional group co-existing in one molecule, and a variety of catalyst systems formed by combination of chiral catalysts and achiral catalysts, containing the catalysts as shown in the following Formula (IC1)˜Formula (IC6):

wherein, in Formula (IC1), R⁴ is H, CH₃, OEt, Ot-Bu; in Formula (IC2), X¹ is OTf, NTf₂; in Formula (IC5), n is 1-5.
 4. The use according to claim 3, wherein, the C6-C20 substituted phenyl is as shown in Formula (a), the C10-C20 substituted naphthyl is as shown in Formula (b) and (c), the C4-C10 substituted furanyl is as shown in Formula (d) and (e), the C4-C10 substituted thienyl is as shown in Formula (f) and (g), the C4-C10 substituted pyrryl is as shown in Formula (h) and (i), the C5-C10 substituted pyridyl is as shown in Formula (j) to (l);

wherein, for S_((b)) and S_((c)) in Formula (a) to (l), S is a substituent, and the substituent is selected from the group consisting of: same or different halogen; C1-C4 alkyl; C1-C4 alkoxyl; ester group CO₂R, wherein, R=Me, Et, i-Pr, t-Bu, Ph, Bn; cyano group; nitro; acetal group or ketal group; b, c are the amount of the substituents, and b is an integer from 1 to 5 inclusive; c is an integer from 1 to 3 inclusive.
 5. Use of a functionalized silyl cyanide for synthesizing alcohol compounds bearing substituted ketone moiety via tandem nucleophilic addition reaction/functional group transfer reaction, comprising the step of: nucleophilic addition reaction of functionalized silyl cyanide 1aa with a carbonyl compound 3a provides an intermediate 4a which undergoes an intramolecular nucleophilic addition reaction promoted by base I and a hydrolysis reaction promoted by acid I; thereby producing alcohol compounds 5 bearing substituted ketone moiety; wherein, the tandem nucleophilic addition reaction/functional group transfer reaction comprises racemic tandem nucleophilic addition reaction/functional group transfer reaction and asymmetric tandem nucleophilic addition reaction/functional group transfer reaction; the alcohol compounds 5 are in R and/or S configuration; the reaction process is as shown in Scheme (III):

wherein, Z is Cl, Br; R² is selected from C1-C20 alkyl, phenyl, C6-C20 substituted phenyl, naphthyl, C10-C20 substituted naphthyl, furanyl, C4-C10 substituted furanyl, thienyl, C4-C10 substituted thienyl, pyrryl, C4-C10 substituted pyrryl, pyridyl, and C5-C10 substituted pyridyl; R³ is selected from H; C1-C20 alkyl; ester group CO₂R, wherein, R=Me, Et, i-Pr, t-Bu, Ph, Bn; and amide CONR₂, wherein, R=Me, Et, CF₃; the catalyst I is used for catalyzing the tandem nucleophilic addition reaction/functional group transfer reaction between the functionalized silyl cyanide 1aa and the carbonyl compound 3a; for the racemic tandem nucleophilic addition reaction/functional group transfer reaction, the catalyst is the catalyst I′ as recited in claim 3; and the dosage of the catalyst is 0.001-0.5 equivalent relative to the carbonyl compound 3a; for the asymmetric tandem nucleophilic addition reaction/functional group transfer reaction, the catalyst is the catalyst I″ as recited in claim 3; and the dosage of the catalyst is 0.001-0.5 equivalent relative to the carbonyl compound 3a; the base I is a strong base for removing hydrogen adjacent to FG; the acid I is an acidic catalyst used for hydrolyzing C—Si and C═N bond, which is selected from hydrochloric acid, sulfuric acid, acetic acid.
 6. The use according to claim 5, wherein: base I is selected from LDA, NaHMDS, KHMDS; and the dosage of base I is 1.0-3.0 equivalent relative to the intermediate 4a.
 7. Use of functionalized silyl cyanide for total synthesis of (S)-1,3-dihydroxy-3,7-dimethyloct-6-en-2-one, comprising the following steps: the nucleophilic addition reaction of functionalized silyl cyanide 1aa with ketone 6 in the presence of the catalyst I produces an intermediate 7; performing an intramolecular nucleophilic attack of the intermediate 7 using LDA as the base, followed by a hydrolyzation in the presence of hydrochloric acid to afford a compound 8; reacting of the compound 8 and KOAc by substitution reaction, followed by a hydrolyzation in the presence of K₂CO₃, thereby producing the (S)-1,3-dihydroxy-3,7-dimethyloct-6-en-2-one; the reaction process is as shown in Scheme (IV),

wherein, Z is Cl, Br; and the dosage of LDA is 1.0-3.0 equivalent relative to the intermediate
 7. 8. Use of functionalized silyl cyanidein tandem cyanosilylation reaction/ring-closing olefin metathesis reaction, comprising the following steps: reacting of functionalized silyl cyanide lab and an alkenyl ketone 9 by cyanosilylation reaction in the presence of the catalyst I to produce an intermediate 10; performing an intramolecular ring-closing olefin metathesis reaction of the intermediate compound 10 in the presence of Grubbs I, thereby producing a silicon-containing heterocyclic compound 11; wherein, the tandem cyanosilylation reaction/ring-closing olefin metathesis reaction comprises racemic cyanosilylation reaction/ring-closing olefin metathesis reaction and asymmetric cyanosilylation reaction/ring-closing olefin metathesis reaction; and the silicon-containing heterocyclic compound 11 is in R and/or S configuration; and the process of the reaction is shown as in Scheme (V):

wherein, n is 0, 1, or 2; R⁶ is H, Me, Et, Ph; for racemic cyanosilylation reaction/ring-closing olefin metathesis reaction, the catalyst I used for the cyanosilylation reaction is K₂CO₃; and for asymmetric cyanosilylation reaction/ring-closing olefin metathesis reaction, the catalyst I used for the cyanosilylation reaction is IC1.
 9. Use of functionalized silyl cyanide for epoxy ring-opening reaction/functional group transfer reaction, comprising the following steps: reacting the functionalized silyl cyanide 1aa and an epoxy compound 12 in the presence of a catalyst I by epoxy ring-opening reaction to produce an intermediate 13; performing an intramolecular nucleophilic attack of the intermediates compound 13 under the promotion of LDA followed by a hydrolyzation mediated by hydrochloric acid to afford an alcohol compound 14; wherein, the epoxy ring-opening reaction/functional group transfer reaction comprises racemic epoxy ring-opening addition reaction/functional group transfer reaction and asymmetric epoxy ring-opening reaction/functional group transfer reaction; and the alcohol compounds 14 is in R and/or S configuration; and the process of the reaction is as shown in Scheme (VI):

wherein, Z is Cl, Br; the catalyst I is used for catalyzing the nucleophilic addition reaction between the functionalized silyl cyanide 1aa and the epoxy compound 12; for the racemic epoxy ring-opening reaction/functional group transfer reaction, the catalyst is the catalyst I′ as recited in claim 3; and the dosage of the catalyst is 0.001-0.5 equivalent relative to the epoxy compound 12; for the asymmetric epoxy ring-opening reaction/functional group transfer reaction, the catalyst is the catalyst I″ as recited in claim 3; and the dosage of the catalyst is 0.001-0.5 equivalent relative to the epoxy compound 12; R⁷ is selected from Me, Ph, Bn, BnCH₂; R⁸ and R⁹ are H, Me, Et, Allyl; wherein, R⁸ and R⁹ can be the same or different.
 10. A compound, having the following structural Formula (7),

wherein, Z is Cl, Br. 